Prof. Akio Kamimura

【Original Articles】

  1. Hydrodecyanation of Secondary Alkyl Nitriles and Malononitriles to Alkanes using DiMeImd-BH3.
    Kawamoto, T.; Oritani, K.; Kawabata, A.; Morioka, T.; Matsubara, H.; Kamimura, A.
    J. Org. Chem. 2020, 85, 6137.
    http://dx.doi.org/10.1021/acs.joc.0c00105

  2. Highly Cumulated Radical Cascade Reaction of aza-1,6-Enyenes: Stereoselective Synthesis of exo-Methylene Piperidines.
    Kamimura, A.; Itaya, T.; Yoshinaga, T.; Nozawa, R.; Kawamoto, T.; Sumimoto, M.; Uno, H.
    Eur. J. Org. Chem. 2020, 700.
    http://dx.doi.org/10.1002/ejoc.202000034

  3. 2‐Sulfanylhydroquinone Dimer as a Switchable Fluorescent Dye.
    Kamimura, A.; Sakamoto, S.; Umemoto, H.; Kawamoto, T.; Sumimoto, M.
    Chem. Eur. J. 2019, 25, 14081.
    http://dx.doi.org/10.1002/chem.201903436

    Selected as Cover Feature
    http://dx.doi.org/10.1002/chem.201904089

  4. Kawamoto, T.; Sasaki, R.; Kamimura, A.; Matsubara, H.
    The regioselective trifluoromethylation of 1,3-bis(vinyl triflates) in the absence of external trifluoromethyl sources.
    J. Fluorine Chem. 2019, 221, 66–69.
    http://dx.doi.org/10.1016/j.jfluchem.2019.04.002

  5. Kamimura, A.; Shiramatsu, Y.; Kawamoto, T.
    Depolymerization of polyamide 6 in hydrophilic ionic liquids.
    Green Energy and Environment 2019, in press.
    http://dx.doi.org/10.1016/j.gee.2019.01.002

  6. Kamimura, A.; Yoshinaga, T.; Miyazaki, K.; Kawamoto, T.
    Comparison of homofugality among alkyl groups attached to tin atom.
    Heteroatom Chem. 2018, 2, e21469–7. http://dx.doi.org/10.1002/hc.21469

  7. Hayashi, Y.; Kranidiotis-Hisatomi, N.; Sakamoto, D.; Oritani, K.; Kawamoto, T.; Kamimura, A.
    Asymmetric Michael Reaction of Aldehydes and Dicyanoalkenes Catalyzed by Diphenylprolinol Silyl Ether.
    Eur. J. Org. Chem. 2018, 6843–6847. http://dx.doi.org/10.1002/ejoc.201800831

  8. Development of a microwave-assisted sustainable conversion of furfural hydrazones to functionalised phthalimides in ionic liquids.
    Karaluka, V.; Murata, K.; Masuda, S.; Shiramatsu, Y.; Kawamoto, T.; Hailes, H. C.; Sheppard, T. D.; Kamimura, A.
    RSC Adv. 2018, 8, 22617–22624. http://dx.doi.org/10.1039/C8RA03895C

  9. Solubility-switchable ionic liquids: A control of hydrophilicity and hydrophobicity using a protective group.
    Kamimura, A.; Shiramatsu, Y.; Murata, K.; Kawamoto, T.
    Chem. Lett. 2018, 47, 1079–1081. http://dx.doi.org/10.1246/cl.180382

  10. Deltaarenes; novel macrocyclic molecules that are readily available from 1,4-benzoquinone and benzene dithiols.
    Kamimura, A.; Watanabe, R.; Fukumitsu, T.; Ikeda, K.; Kawamoto, T.; Sumimoto, M.; Mori, S.; Uno, H.
    Tetrahedron 2018, 74, 5303–5308. http://dx.doi.org/10.1016/j.tet.2018.04.070

  11. Thiol-Catalyzed Radical Decyanation of Aliphatic Nitriles with Sodium Borohydride
    Kawamoto, T.; Oritani, K.; Curran, D. P.; Kamimura, A.
    Org. Lett. 2018, 20, 2084–2087. https://dx.doi.org/10.1021/acs.orglett.8b00626
             
  12. Tris (trimethylsilyl) silane-Mediated Reductive Decyanation and Cyano Transfer Reactions of Malononitriles
    Kawamoto, T.; Shimaya, Y.; Curran, D. P.; Kamimura, A.
    Chem. Lett. 2018, 47, 573–575. https://doi.org/10.1246/cl.171231

  13. A kinetic study on the conversion of nylon 12 to methyl 12-hydroxydodecanoate in supercritical MeOH in the presence of carboxylic acid
    Kamimura, A.; Ikeda, K.; Suzuki, S.; Kato, K.; Matsumoto, H.; Kaiso, K.; Yoshimoto, M.
    Polym. Degr. Stabil.
    2017, 146, 95–104. http://dx.doi.org/10.1016/j.polymdegradstab.2017.09.015
  14. An efficient and selective conversion of sorbitol in ionic liquids: Use of ion exchange resin as a solid acid catalyst
    Kamimura, A.; Murata, K.; Kawamoto, T.
    Tetrahedron Lett.
    2017, 58, 3616–3618. http://dx.doi.org/10.1016/j.tetlet.2017.07.105
  15. Preparation of 2,3-trans-substituted piperidines from optically active β-amino-α-methylene esters: Synthesis of optically active (2S,3R)-(−)-epi-CP-99,994
    Kamimura, A.; Yo, R.; Uno, H.
    Tetrahedron
    2017, 73, 4770–4778. http://dx.doi.org/10.1016/j.tet.2017.06.054
  16. Synthesis of α-Trifluoromethylated Ketones from Vinyl Triflates in the Absence of External Trifluoromethyl Sources
    Kawamoto, T.; Sasaki, R.; Kamimura, A.
    Angew. Chem. Int. Ed.
    2017, 56, 1342–1345. http://dx.doi.org/10.1002/anie.201608591
  17. Efficient depolymerization and chemical conversion of polyamide 66 to 1,6-hexanediol
    Matsumoto, H.; Akinari, Y.; Kaiso, K.; Kamimura, A.
    J. Mater. Cycles Waste Manag.
    2017, 19, 326–331. http://dx.doi.org/10.1007/s10163-015-0425-4
  18. Modulation of cellulase activity by charged lipid bilayers with different acyl chain properties for efficient hydrolysis of ionic liquid-pretreated cellulose
    Mihono, K.; Ohtsu, T.; Ohtani, M.; Yoshimoto, M.; Kamimura, A.
    Colloids Surface B
    2016, 146, 198–203. http://dx.doi.org/10.1016/j.colsurfb.2016.06.005
  19. Asymmetric Synthesis of Bicyclic Nitrocyclopropanes from Primary Nitro Compounds and Stereoselective Formation of Tetrahydro-2H-cyclopenta[b]furans via Ring Expansion/Cyclization Reaction
    Kamimura, A.; Moriyama, T.; Ito, Y.; Kawamoto, T.; Uno, H.
    J. Org. Chem.
    2016, 81, 4664–4681. http://dx.doi.org/10.1021/acs.joc.6b00566
  20. A radical cascade reaction triggered by thiyl radical; An approach toward synthesis of tricyclic structure of platensimycin
    Kamimura, A.; Kawakami, Y.
    Phosphous, Sulfur Silicon Relat. Elem.
    2016, 191, 259–262. http://dx.doi.org/10.1080/10426507.2015.1064922
  21. A radical cascade reaction of aza-1,6-enyne compounds using allyltributyltin
    Kamimura, A.; Miyazaki, K.; Kawamoto, T.; Uno, H.
    Tetrahedron
    2016, 72, 7722–7726. http://dx.doi.org/10.1016/j.tet.2016.04.078
  22. Oxidative synthesis of isoxazoline-N-oxide from optically active nitro alcohols
    Moriyama, T.; Kawamoto, T.; Uno, H.; Kamimura, A.
    Heterocycles
    2016, 92, 1479–1489. http://dx.doi.org/10.3987/COM-16-13497
  23. An efficient conversion of lysine to 2-aminocaprolactam
    Matsumoto, H.; Kaiso, K.; Kamimura, A.
    Heterocycles
    2016, 92, 337–345. http://dx.doi.org/10.3987/COM-15-13358
  24. Synthesis of 6-Arylpyridin-3-ols by Oxidative Rearrangement of (5-Arylfurfuryl)amines
    Fürst, M.C.D.; Sauer, C.S.; Moriyama, T.; Kamimura, A.; Heinrich, M.R.
    Eur. J. Org. Chem.
    2016, 2016, 3051–3055. http://dx.doi.org/10.1002/ejoc.201600377
     
  25. An oxidative cyclopropanation reaction of primary nitro compounds using Fe2O3
    Moriyama, T.; Ito, Y.; Koyama, Y.; Kawamoto, T.; Kamimura, A.
    Tetrahedron Lett.
    2016, 57, 3127–3128. http://dx.doi.org/10.1016/j.tetlet.2016.06.013
     
  26. A regioselective double Stille coupling reaction of bicyclic stannolanes
    Kamimura, A.; Tanaka, T.; So, M.; Itaya, T.; Matsuda, K.; Kawamoto, T.
    Org. Biomol. Chem.
    2016, 14, 8109–8122. http://dx.doi.org/10.1039/c6ob01018k
  27. Synthesis of unsymmetrical 3,7-bisarylthio-2,8-dioxydibenzofuran and its physical properties
    Kamimura, A.; Ishikawa, M.; Watanabe, R.; Sakamoto, S.; Uno, H.
    Phosphous, Sulfur Silicon Relat. Elem.
    2015, 190, 1219–1224. http://dx.doi.org/10.1080/10426507.2014.983598
  28. Synthesis of dibenzo[c,e][1,2]diazocines - A new group of eight-membered cyclic azo compounds
    Nokubi, T.; Kindt, S.; Clark, T.; Kamimura, A.; Heinrich, M.R.
    Tetrahedron Lett.
    2015, 56, 316–320. http://dx.doi.org/10.1016/j.tetlet.2014.11.064
  29. A mechanistic study on the SHi reaction at tin atoms in a radical cascade reaction
    Kamimura, A.; Yoshinaga, T.; Noguchi, F.; Miyazaki, K.; Uno, H.
    Org. Chem. Front.
    2015, 2, 713–720. http://dx.doi.org/10.1039/c5qo00063g
  30. Preparation of hydrophobic 2-phenylthiohydroquinone dimers and evaluation of their photophysical properties
    Kamimura, A.; Takechi, Y.; Watanabe, R.
    Heteroatom Chem.
    2014, 25, 402–409. http://dx.doi.org/10.1002/hc.21169
  31. Preparation of 2,3-dihydrofurans via a double allylic substitution reaction of allylic nitro compounds
    Nakano, T.; Miyazaki, K.; Kamimura, A.
    J. Org. Chem.
    2014, 79, 8103–8109. http://dx.doi.org/10.1021/jo5013042
  32. Gold(I)-catalyzed synthesis of optically active 1,4-oxazepan-7-ones
    Kamimura, A.; Yamane, Y.; Yo, R.; Tanaka, T.; Uno, H.
    J. Org. Chem.
    2014, 79, 7696–7702. http://dx.doi.org/10.1021/jo501254x
  33. 不斉Aza-Morita-Baylis-Hillman等価反応を用いた複素環の合成
    上村明男・石川慎吾
    有機合成化学協会誌 2014, 72, 929–939. http://dx.doi.org/10.5059/yukigoseikyokaishi.72.929
  34. 4,4′-diarylsulfanyl-2,2′,5,5′-tetraoxybiaryl derivatives as a water-soluble fluorescent dye
    Kamimura, A.; Nokubi, T.; Watanabe, R.; Ishikawa, M.; Nasu, K.; Uno, H.; Sumimoto, M.
    J. Org. Chem.
    2014, 79, 1068–1083. http://dx.doi.org/10.1021/jo402522y
  35. Rapid conversion of sorbitol to isosorbide in hydrophobic ionic liquids under microwave irradiation
    Kamimura, A.; Murata, K.; Tanaka, Y.; Okagawa, T.; Matsumoto, H.; Kaiso, K.; Yoshimoto, M.
    ChemSusChem
    2014, 7, 3257–3259. http://dx.doi.org/10.1002/cssc.201402655
  36. Efficient Conversion of Polyamides to ω-Hydroxyalkanoic Acids: A New Method for Chemical Recycling of Waste Plastics
    Kamimura, A.; Ikeda, K.; Suzuki, S.; Kato, K.; Akinari, Y.; Sugimoto, T.; Kashiwagi, K.; Kaiso, K.; Matsumoto, H.; Yoshimoto, M.
    ChemSusChem
    2014, 7, 2473–2477. http://dx.doi.org/10.1002/cssc.201402125
  37. A rapid route to aminocyclopropanes via carbamatoorganozinc carbenoids
    Ishikawa, S.; Sheppard, T.D.; D'Oyley, J.M.; Kamimura, A.; Motherwell, W.B.
    Angew. Chem. Int. Ed.
    2013, 52, 10060–10063. http://dx.doi.org/10.1002/anie.201304720
  38. Hydrolysis of insoluble cellulose to glucose catalyzed by cellulase-containing liposomes in an aqueous solution of 1-butyl-3-methylimidazolium chloride
    Yoshimoto, M.; Tanimura, K.; Tokunaga, K.; Kamimura, A.
    Biosci. Biotech. Biochem.
    2013, 29, 1190–1196. http://dx.doi.org/10.1002/btpr.1779
  39. A new water-soluble fluorescent dye based on 2-sulfanylhydroquinone dimers
    Nokubi, T.; Nasu, K.; Watanabe, R.; Kamimura, A.
    Chem. Lett.
    2013, 42, 876–878. http://dx.doi.org/10.1246/cl.130348
  40. A radical cascade cyclization to prepare dihydrothiophenes induced by thiyl radicals as sulfur biradical equivalents
    Kamimura, A.; Miyazaki, K.; Yamane, Y.; Yo, R.; Ishikawa, S.; Uno, H.; Sumimoto, M.
    J. Org. Chem.
    2013, 78, 7816–7822. http://dx.doi.org/10.1021/jo400975t
  41. Sub-stoichiometric oxidation of benzylic alcohols with commercially available activated MnO2under oxygen atmosphere: A green modification of the benzylic oxidation
    Kamimura, A.; Komatsu, H.; Moriyama, T.; Nozaki, Y.
    Tetrahedron
    2013, 69, 5968–5972. http://dx.doi.org/10.1016/j.tet.2013.04.109
  42. Preparation of optically active bicyclodihydrosiloles by a radical cascade reaction
    Miyazaki, K.; Yamane, Y.; Yo, R.; Uno, H.; Kamimura, A.
    Beilstein J. Org. Chem.
    2013, 9, 1326–1332. http://dx.doi.org/10.3762/bjoc.9.149
  43. Kinetic study of the 7- endo selective radical cyclization of N-tert-butyl-o-bromobenzylmethacryl amides: Kinetic investigation of the cyclization and 1,7-hydrogen transfer of aromatic radicals
    Kamimura, A.; Kotake, T.; Ishihara, Y.; So, M.; Hayashi, T.
    J. Org. Chem.
    2013, 78, 3961–3971. http://dx.doi.org/10.1021/jo400326b
  44. Unexpected reductive double carbon-carbon bonds cleavage of bicyclic nitrocyclopropanes
    Kamimura, A.; Ikeda, K.; Moriyama, T.; Uno, H.
    Tetrahedron Lett.
    2013, 54, 1842–1844. http://dx.doi.org/10.1016/j.tetlet.2013.01.094
  45. Preparation of optically active 4-aminopyrrolidines by radical addition/cyclization to chiral n-(2-(methoxyimino)ethyl)-β-amino-α- methylene esters
    Kamimura, A.; Yamane, Y.; Uno, H.
    Phosphous, Sulfur Silicon Relat. Elem.
    2013, 188, 356–366. http://dx.doi.org/10.1080/10426507.2012.736893
  46. Pd-catalyzed tandem sp2-sp3 coupling reactions of chiral stannolanes: An efficient preparation of optically active tetrahydrobenz[f]isoindoles
    Kamimura, A.; So, M.; Ishikawa, S.; Uno, H.
    Org. Lett.
    2013, 15, 1402–1405. http://dx.doi.org/10.1021/ol4003948
  47. Oxidation of benzyl alcohols by semi-stoichiometric amounts of cobalt-doped birnessite-type layered MnO2 under oxygen atmosphere
    Kamimura, A.; Nozaki, Y.; Nishiyama, M.; Nakayama, M.
    RSC Adv.
    2013, 3, 468–472. http://dx.doi.org/10.1039/c2ra22117a
  48. Combination use of hydrophobic ionic liquids and LiCl as a good reaction system for the chemical conversion of cellulose to glucose
    Kamimura, A.; Okagawa, T.; Oyama, N.; Otsuka, T.; Yoshimoto, M.
    Green Chem.
    2012, 14, 2816–2820. http://dx.doi.org/10.1039/c2gc35811e
  49. Nylon 6 depolymerization in supercritical alcohols studied by the QM/MC/FEP method
    Kaweetirawatt, T.; Yamaguchi, T.; Hayashiyama, S.; Sumimoto, M.; Kamimura, A.; Hori, K.
    RSC Adv.
    2012, 2, 8402–8409. http://dx.doi.org/10.1039/c2ra20835k
  50. A study on the relationship between the twisted π-conjugate system of 1,5-diaryl-1,5-diazapenta-1,3-dienes and their photophysical properties
    Kamimura, A.; Matsu, H.; Suzukawa, H.; Sato, E.; Sumimoto, M.; Uno, H.
    Chem. Lett.
    2012, 41, 984–986. http://dx.doi.org/10.1246/cl.2012.984
  51. Facile synthesis of quinone dimer derivatives substituted with sulfanyl groups and their properties
    Kamimura, A.; Nokubi, T.; Nasu, K.; Takechi, Y.; Ishihara, Y.; Kato, K.; Noguchi, S.; Watanabe, M.; Shirai, M.; Sumimoto, M.; Uno, H.
    Chem. Lett.
    2012, 41, 950–951. http://dx.doi.org/10.1246/cl.2012.950
  52. Unexpected formation of stannolanes and trigonal bipyramidal tin complexes by radical cyclization reaction
    Kamimura, A.; Ishikawa, S.; Noguchi, F.; Moriyama, T.; So, M.; Murafuji, T.; Uno, H.
    Chem. Commun.
    2012, 48, 6592–6594. http://dx.doi.org/10.1039/c2cc31753b
  53. Total synthesis of ent-calystegine B4 via nitro-Michael/aldol reaction
    Kamimura, A.; Miyazaki, K.; Suzuki, S.; Ishikawa, S.; Uno, H.
    Org. Biomol. Chem.
    2012, 10, 4362–4366. http://dx.doi.org/10.1039/c2ob25386k
  54. Preparation of S RN1-type coupling adducts from aliphatic gem-dinitro compounds in ionic liquids
    Kamimura, A.; Toyoshima, S.
    Molecules
    2012, 17, 4782–4790. http://dx.doi.org/10.3390/molecules17054782
  55. Concise synthesis of 2-benzazepine derivatives and their biological activity
    So, M.; Kotake, T.; Matsuura, K.; Inui, M.; Kamimura, A.
    J. Org. Chem.
    2012, 77, 4017–4028. http://dx.doi.org/10.1021/jo300380z
  56. Heck-Matsuda reaction for allylic nitro compounds: A short asymmetric synthesis of an FTY720 derivative
    Nakano, T.; Miyahara, M.; Itoh, T.; Kamimura, A.
    Eur. J. Org. Chem.
    2012, 2161–2166. http://dx.doi.org/10.1002/ejoc.201101703
  57. Stereoselective synthesis of 1-nitrobicyclo[3.1.0]hexanes and fused isoxazoline-N-oxides from primary nitro compounds
    Kamimura, A.; Takeuchi, R.; Ikeda, K.; Moriyama, T.; Sumimoto, M.
    J. Org. Chem.
    2012, 77, 2236–2245. http://dx.doi.org/10.1021/jo202489v
  58. Direct conversion of polyamides to ω-hydroxyalkanoic acid derivatives by using supercritical MeOH
    Kamimura, A.; Kaiso, K.; Suzuki, S.; Oishi, Y.; Ohara, Y.; Sugimoto, T.; Kashiwagi, K.; Yoshimoto, M.
    Green Chem.
    2011, 13, 2055–2061. http://dx.doi.org/10.1039/c1gc15172j
  59. Depolymerization of unsaturated polyesters and waste fiber-reinforced plastics by using ionic liquids: The use of microwaves to accelerate the reaction rate
    Kamimura, A.; Yamamoto, S.; Yamada, K.
    ChemSusChem
    2011, 4, 644–649. http://dx.doi.org/10.1002/cssc.201000430
  60. Effective depolymerization of nylon-6 in wet supercritical hydrocarbons
    Kaiso, K.; Sugimoto, T.; Kashiwagi, K.; Kamimura, A.
    Chem. Lett.
    2011, 40, 370–371. http://dx.doi.org/10.1246/cl.2011.370
  61. K-birnessite MnO2: A new selective oxidant for benzylic and allylic alcohols
    Kamimura, A.; Nozaki, Y.; Ishikawa, S.; Inoue, R.; Nakayama, M.
    Tetrahedron Lett.
    2011, 52, 538–540. http://dx.doi.org/10.1016/j.tetlet.2010.11.114
  62. Chemo-Enzymatic Synthesis of a Multi-Useful Chiral Building. Block Molecule for the Synthesis of Medicinal Compounds
    Nakano, T.; Yagi, Y.; Miyahara, M.; Kaminura, A.; Kawatsura, M.; Itoh, T.
    Molecules 2011, 16, 6747–6757. https://doi.org/10.3390/molecules16086747
  63. Surfactant-induced electrodeposition of layered manganese oxide with large interlayer space for catalytic oxidation of phenol
    Nakayama, M.; Shamoto, M.; Kamimura, A.
    Chem. Mater.
    2010, 22, 5887–5894. http://dx.doi.org/10.1021/cm101970b
  64. Improved preparation of recycled polymers in chemical recycling of fiber-reinforced plastics and molding of test product using recycled polymers
    Yamada, K.; Tomonaga, F.; Kamimura, A.
    J. Mater. Cycles Waste Manag.
    2010, 12, 271–274. http://dx.doi.org/10.1007/s10163-010-0296-7
  65. Efficient chemical recycling of waste fiber-reinforced plastics: Use of reduced amounts of dimethylaminopyridine and activated charcoal for the purification of recovered monomer
    Kamimura, A.; Akinari, Y.; Watanabe, T.; Yamada, K.; Tomonaga, F.
    J. Mater. Cycles Waste Manag.
    2010, 12, 93–97. http://dx.doi.org/10.1007/s10163-010-0276-y
  66. Asymmetric synthesis of 2-alkyl-substituted 2,5-dihydropyrroles from optically active aza-baylis-hillman adducts. Formal synthesis of (-)-trachelanthamidine
    Ishikawa, S.; Noguchi, F.; Kamimura, A.
    J. Org. Chem.
    2010, 75, 3578–3586. http://dx.doi.org/10.1021/jo100315j
  67. Use of the diels-alder adduct of pyrrole in organic synthesis. Formal racemic synthesis of tamiflu
    Kamimura, A.; Nakano, T.
    J. Org. Chem.
    2010, 75, 3133–3136. http://dx.doi.org/10.1021/jo1002856
  68. Intramolecular Pauson-Khand reaction of optically active aza-Baylis-Hillman adducts
    Ishikawa, S.; Noguchi, F.; Uno, H.; Kamimura, A.
    Tetrahedron Lett.
    2010, 51, 2329–2331. http://dx.doi.org/10.1016/j.tetlet.2010.02.115
  69. Stereoselective synthesis of bicyclic nitrocyclopropanes by a radical-anion domino reaction
    Kamimura, A.; Kadowaki, A.; Yoshida, T.; Takeuchi, R.; Uno, H.
    Chem. Eur. J.
    2009, 15, 10330–10334. http://dx.doi.org/10.1002/chem.200901920
  70. Preparation of novel functionalized ammonium salts that effectively catalyze depolymerization of Nylon-6 in ionic liquids
    Yamamoto, S.; Kamimura, A.
    Chem. Lett.
    2009, 38, 1016–1017. http://dx.doi.org/10.1246/cl.2009.1016
  71. An efficient preparation of N-alkyl-2-benzazepine derivatives and investigation of their biological activity
    Kamimura, A.; So, M.; Kuratani, T.; Matsuura, K.; Inui, M.
    Bioorg. Med. Chem. Lett.
    2009, 19, 3193–3195. http://dx.doi.org/10.1016/j.bmcl.2009.04.117
  72. Improved method for the formation of recycled resins from depolymerized products of waste fiber-reinforced plastics: Simple and effective purification of recovered monomers by washing with water
    Kamimura, A.; Konno, E.; Yamamoto, S.; Watanabe, T.; Yamada, K.; Tomonaga, F.
    J. Mater. Cycles Waste Manag.
    2009, 11, 133–137. http://dx.doi.org/10.1007/s10163-008-0225-1
  73. Mechanistic study of 7-endo selective radical cyclization of the aryl radical
    Kamimura, A.; Ishihara, Y.; So, M.; Hayashi, T.
    Tetrahedron Lett.
    2009, 50, 1727–1730. http://dx.doi.org/10.1016/j.tetlet.2009.01.132
  74. Formation of recycled plastics from depolymerized monomers derived from waste fiber-reinforced plastics
    Kamimura, A.; Konno, E.; Yamamoto, S.; Watanabe, T.; Yamada, K.; Tomonaga, F.
    J. Mater. Cycles Waste Manag.
    2009, 11, 38–41. http://dx.doi.org/10.1007/s10163-008-0217-1
  75. A novel depolymerization of nylons in ionic liquids
    Kamimura, A.; Yamamoto, S.
    Polym. Adv. Technol.
    2008, 19, 1391–1395. http://dx.doi.org/10.1002/pat.1199
  76. Stereoselective synthesis of azepines through the conjugate addition of formamides to nitroalkenes and subsequent intramolecular nitrile oxide cycloaddition reaction
    Kamimura, A.; Yoshida, T.; Uno, H.
    Tetrahedron
    2008, 64, 11081–11085. http://dx.doi.org/10.1016/j.tet.2008.09.070
  77. DMAP as an effective catalyst to accelerate the solubilization of waste fiber-reinforced plastics
    Kamimura, A.; Yamada, K.; Kuratani, T.; Oishi, Y.; Watanabe, T.; Yoshida, T.; Tomonaga, F.
    ChemSusChem
    2008, 1, 845–850. http://dx.doi.org/10.1002/cssc.200800151
  78. Supercritical secondary alcohols as useful media to convert polyamide into monomeric lactams
    Kamimura, A.; Oishi, Y.; Kaiso, K.; Sugimoto, T.; Kashiwagi, K.
    ChemSusChem
    2008, 1, 82–84. http://dx.doi.org/10.1002/cssc.200700024
  79. 有機触媒と超臨界アルコールを用いたFRPの化学リサイクル
    上村明男, 友永文昭, 山田和男
    化学工業 2008, 59, 560–568.
  80. 超臨界流体とイオン液体を使った新しいプラスチックの解重合反応―有機合成化学の新しい応用
    上村明男
    Chemical Times 2008, 208, 2–8.
  81. Stereoselective conjugate addition of lactams to nitroalkenes and formal total synthesis of indolizidine 167B
    Kamimura, A.; Nagata, Y.; Kadowaki, A.; Uchida, K.; Uno, H.
    Tetrahedron
    2007, 63, 11856–11861. http://dx.doi.org/10.1016/j.tet.2007.09.023
  82. An efficient method to depolymerize polyamide plastics: A new use of ionic liquids
    Kamimura, A.; Yamamoto, S.
    Org. Lett.
    2007, 9, 2532–2535. http://dx.doi.org/10.1021/ol070886c
  83. Promotion of skin epithelial cell migration and wound healing by a 2-benzazepine derivative
    Matsuura, K.; Kuratani, T.; Gondo, T.; Kamimura, A.; Inui, M.
    Eur. J. Pharmacol.
    2007, 563, 83–87. http://dx.doi.org/10.1016/j.ejphar.2007.02.014
  84. Asymmetric thio-Michael/nucleophilic addition domino reaction with chiral N-sulfinimines
    Kamimura, A.; Okawa, H.; Morisaki, Y.; Ishikawa, S.; Uno, H.
    J. Org. Chem.
    2007, 72, 3569–3572. http://dx.doi.org/10.1021/jo062251h
  85. Stereoselective intramolecular 1,3-dipolar nitrile oxide cycloaddition reaction of N-formyl-β-nitroamides
    Kadowaki, A.; Nagata, Y.; Uno, H.; Kamimura, A.
    Tetrahedron Lett.
    2007, 48, 1823–1825. http://dx.doi.org/10.1016/j.tetlet.2007.01.025
  86. Effective depolymerization waste FRPs by treatment with DMAP and supercritical alcohol
    Kamimura, A.; Yamada, K.; Kuratani, T.; Taguchi, Y.; Tomonaga, F.
    Chem. Lett.
    2006, 35, 586–587. http://dx.doi.org/10.1246/cl.2006.586
  87. A convenient synthesis of medium-sized lactams through RCM reaction of oxyoxazolidinones
    Kamimura, A.; Tanaka, K.; Hayashi, T.; Omata, Y.
    Tetrahedron Lett.
    2006, 47, 3625–3627. http://dx.doi.org/10.1016/j.tetlet.2006.03.152
  88. Formamide as an efficient nitrogen nucleophile for the Michael addition to nitroalkenes
    Kamimura, A.; Kadowaki, A.; Nagata, Y.; Uno, H.
    Tetrahedron Lett.
    2006, 47, 2471–2473. http://dx.doi.org/10.1016/j.tetlet.2006.02.065
  89. Regioselective Michael addition of thiols to unsymmetrical fumaric diesters or esteramides
    Kamimura, A.; Murakami, N.; Suzukawa, H.; Kawahara, F.
    Phosphous, Sulfur Silicon Relat. Elem.
    2005, 180, 1467–1468. http://dx.doi.org/10.1080/10426500590913113
  90. A practical method for chemical recycling of FRP. DMAP as an effective catalyst for degradation of FRPs in supercritical alcohol
    Kamimura, A.; Kuratani, T.; Yamada K.; Tomonaga, F.
    Feedstock recycling of Plastics, Selected Papers presented at the Third International Symposium on Feedstock Recycling of Plastics, Muller-Hagedorn, M.; Blckhorn, H. Eds. Universitatsverlag Karlsruhe, 2005, 525–529.
  91. チオールの共役付加を用いた高選択的炭素骨格構築法の開発
    上村明男
    硫酸と工業, 2005, 58, 162–168.
  92. Convenient switching of 7-endo/6-exo radical cyclization
    Kamimura, A.; Taguchi, Y.
    Tetrahedron Lett.
    2004, 45, 2335–2337. http://dx.doi.org/10.1016/j.tetlet.2004.01.090
  93. 硫黄およびセレン求核剤を用いるマイケル付加反応の新展開
    Kamimura, A.
    有機合成化学協会誌 2004, 62, 705–715. http://dx.doi.org/10.5059/yukigoseikyokaishi.62.705
  94. A convenient stereoselective synthesis of β-lactams from β-hydroxy-α-thioalkylesters prepared from Michael/aldol tandem reaction or stereoselective addition of thiols to the Baylis-Hillman adducts
    Kamimura, A.; Morita, R.; Matsuura, K.; Mitsudera, H.; Shirai, M.
    Tetrahedron
    2003, 59, 9931–9938. http://dx.doi.org/10.1016/j.tet.2003.10.035
  95. On the regioselectivity for the Michael addition of thiols to unsymmetrical fumaric derivatives
    Kamimura, A.; Murakami, N.; Kawahara, F.; Yokota, K.; Omata, Y.; Matsuura, K.; Oishi, Y.; Morita, R.; Mitsudera, H.; Suzukawa, H.; Kakehi, A.; Shirai, M.; Okamoto, H.
    Tetrahedron
    2003, 59, 9537–9546. http://dx.doi.org/10.1016/j.tet.2003.10.007
  96. Oxyoxazolidinone as an auxiliary for heterocyclic synthesis. Enantioselective formation of N-unprotected 2-pyrrolidones from selenocarboxylate and allylamines via radical cyclization
    Kamimura, A.; Omata, Y.; Tanaka, K.; Shirai, M.
    Tetrahedron
    2003, 59, 6291–6299. http://dx.doi.org/10.1016/S0040-4020(03)01015-9
  97. Convenient synthesis of 2-benzazepines via radical cyclization
    Kamimura, A.; Taguchi, Y.; Omata, Y.; Hagihara, M.
    J. Org. Chem.
    2003, 68, 4996–4998. http://dx.doi.org/10.1021/jo030052h
  98. Magnesium cation-induced anti-aldol selective tandem Michael/aldol reaction
    Kamimura, A.; Mitsudera, H.; Omata, Y.; Matsuura, K.; Shirai, M.; Kakehi, A.
    Tetrahedron
    2002, 58, 9817–9826. http://dx.doi.org/10.1016/S0040-4020(02)01299-1
  99. Enantioselective preparation of 3,4,5-trisubstituted 4,5-dihydroisoxazoles and their stereoselective elaboration of 5-side chain
    Kamimura, A.; Kaneko, Y.; Ohta, A.; Matsuura, K.; Fujimoto, Y.; Kakehi, A.; Kanemasa, S.
    Tetrahedron
    2002, 58, 9613–9620. http://dx.doi.org/10.1016/S0040-4020(02)01255-3
  100. Stereoselective formation of optically active 2-oxy-1,3-oxazolidin-4-ones from chiral O-acylmandelamides or lactamides
    Kamimura, A.; Omata, Y.; Kakehi, A.; Shirai, M.
    Tetrahedron
    2002, 58, 8763–8770. http://dx.doi.org/10.1016/S0040-4020(02)01057-8
  101. Regioselective Michael addition of thiols to tertiary fumaric amide esters
    Kamimura, A.; Murakami, N.; Yokota, K.; Shirai, M.; Okamoto, H.
    Tetrahedron Lett.
    2002, 43, 7521–7523. http://dx.doi.org/10.1016/S0040-4039(02)01824-5
  102. Stereoselective formation of optically active 2-oxy-1,3-oxazolidin-4-ones and an efficient synthesis of optically active secondary 2-pyrrolidones
    Omata, Y.; Kakehi, A.; Shirai, M.; Kamimura, A.
    Tetrahedron Lett.
    2002, 43, 6911–6914. http://dx.doi.org/10.1016/S0040-4039(02)01632-5
     
  103. Simple preparation of β-hydroxy-α-thiomethyl carbonyl compounds via stereoselective conjugate addition of thiol to Baylis-Hillman adducts
    Kamimura, A.; Morita, R.; Matsuura, K.; Omata, Y.; Shirai, M.
    Tetrahedron Lett.
    2002, 43, 6189–6191. http://dx.doi.org/10.1016/S0040-4039(02)01318-7
  104. Stereoselective construction of multi-substituted tetrahydrofurans via three components-condensation reaction
    Kamimura, A.; Mitsudera, H.; Matsuura, K.; Omata, Y.; Shirai, M.; Yokoyama, S.; Kakehi, A.
    Tetrahedron
    2002, 58, 2605–2611. http://dx.doi.org/10.1016/S0040-4020(02)00135-7
  105. Regioselective conjugate addition of thiols to unsymmetric fumaric esters in the presence of a lithium cation
    Kamimura, A.; Kawahara, F.; Omata, Y.; Murakami, N.; Morita, R.; Otake, H.; Mitsudera, H.; Shirai, M.; Kakehi, A.
    Tetrahedron Lett.
    2001, 42, 8497–8500. http://dx.doi.org/10.1016/S0040-4039(01)01824-X
  106. Regioselective radical elimination of o-(bromoaryl)sulfides
    Kamimura, A.; Mitsudera, H.
    Tetrahedron Lett.
    2001, 42, 7457–7460. http://dx.doi.org/10.1016/S0040-4039(01)01573-8
  107. A simple preparation of syn-NH-amide aldols and amide-Baylis-Hillman adducts via a Michael-aldol tandem process
    Kamimura, A.; Omata, Y.; Mitsudera, H.; Kakehi, A.
    J. Chem. Soc., Perkin Trans. 1
    2000, 4499–4504. http://dx.doi.org/10.1039/b004721j
  108. An ab initio molecular orbital study on the magnesium controlled 1,3- cycloaddition of nitrile oxides and allylic alcohols with regio- and stereoselectivity
    Fukuda, S.; Kamimura, A.; Kanemasa, S.; Hori, K.
    Tetrahedron
    2000, 56, 1637–1647. http://dx.doi.org/10.1016/S0040-4020(00)00042-9
  109. Synthesis of hydroximoyl chlorides from aldoximes and benzyltrimethylammonium tetrachloroiodate (BTMA ICl4)
    Kanemasa, S.; Matsuda, H.; Kamimura, A.; Kakinami, T.
    Tetrahedron
    2000, 56, 1057–1064. http://dx.doi.org/10.1016/S0040-4020(99)01047-9
  110. Anti-Aldol selective tandem Michael/aldol reaction with magnesium selenolate and stereoselective preparation of tetrasubstituted tetrahydrofuran
    Mitsudera, H.; Kakehi, A.; Kamimura, A.
    Tetrahedron Lett.
    1999, 40, 7389–7392. http://dx.doi.org/10.1016/S0040-4039(99)01516-6
  111. Stereoselective thio-Michael/aldol tandem reaction to α,β-unsaturated esters
    Kamimura, A.; Mitsudera, H.; Asano, S.; Kidera, S.; Kakehi, A.
    J. Org. Chem.
    1999, 64, 6353–6360. http://dx.doi.org/10.1021/jo990548s
  112. Enantioselective preparation of 3,4,5-trisubstituted-4,5- dihydroisoxazoles and 4-substituted-5,6-dihydro-4H-[1,2]-oxazines by nitrile oxide cycloaddition to α-silyl allyl alcohols
    Kamimura, A.; Kaneko, Y.; Ohta, A.; Kakehi, A.; Matsuda, H.; Kanemasa, S.
    Tetrahedron Lett.
    1999, 40, 4349–4352. http://dx.doi.org/10.1016/S0040-4039(99)00688-7
  113. Asymmetric Baylis-Hillman reactions: Catalysis using a chiral pyrrolizidine base
    Barrett, A.G.M.; Cook, A.S.; Kamimura, A.
    Chem. Commun.
    1998, 2533–2534. http://dx.doi.org/
  114. A facile preparation of α-hydrazino-α,β-unsaturated ketones via aza- Baylis-Hillman reaction
    Kamimura, A.; Gunjigake, Y.; Mitsudera, H.; Yokoyama, S.
    Tetrahedron Lett.
    1998, 39, 7323–7324. http://dx.doi.org/10.1016/S0040-4039(98)01570-6
  115. Stereoselective Michael/aldol tandem reaction triggered by thiolate anion or analogues
    Kamimura, A.; Mitsudera, H.; Asano, S.; Kakehi, A.; Noguchi, M.
    Chem. Commun.
    1998, 1095–1096. http://dx.doi.org/
  116. Ab initio molecular orbital study on the mechanism of amide hydrolysis dependent on leaving groups
    Hori, K.; Kamimura, A.; Ando, K.; Mizumura, M.; Ihara, Y.
    Tetrahedron
    1997, 53, 4317–4330. http://dx.doi.org/10.1016/S0040-4020(97)00158-0
  117. Molecular and crystal structure and properties of Te-containing p-terphenoquinone analogues
    Tamura, R.; Takasuka, H.; Nagata, Y.; Azuma, N.; Matsumoto, A.; Sadaoka, Y.; Gunji, A.; Takahashi, K.; Kamimura, A.; Hori, K.
    Mol. Cryst. Liq. Cryst.
    1996, 278-279, 139–150. http://dx.doi.org/
  118. Catalytic asymmetric synthesis of α-methylene-β-hydroxy-ketones
    Barrett, A.G.M.; Kamimura, A.
    J. Chem. Soc., Chem. Commun.
    1995, 1755–1756. http://dx.doi.org/10.1039/C39950001755
  119. Theoretical study on the mechanism of ester hydrolysis in micellar catalysis using model systems
    Hori, K.; Kamimura, A.; Kimoto, J.; Gotoh, S.; Ihara, Y.
    J. Chem. Soc., Perkin Trans. 2
    1994, 2053–2058. http://dx.doi.org/
  120. First Successful Metal Coordination Control in 1, 3-Dipolar Cycloadditions. High-Rate Acceleration and Regio-and Stereocontrol of Nitrile Oxide Cycloadditions to the Magnesium Alkoxides of Allylic and Homoallylic Alcohols
    Kanemasa, S.; Nishiuchi, M.; Kamimura, A.; Hori, K.
    J. Am. Chem. Soc.
    1994, 116, 2324–2339. http://dx.doi.org/10.1021/ja00085a012
  121. Preparation of Chiral Nitroxide Radicals and Spontaneous Optical Resolution by Recrystallization
    Tamura, R.; Susuki, S.; Azuma, N.; Matsumoto, A.; Toda, F.; Kamimura, A.; Hori, K.
    Angew. Chem. Int. Ed.
    1994, 33, 878–879. http://dx.doi.org/10.1002/anie.199408781
  122. Reversing the regiochemical course of 1,3-dipolar cycloaddition of nitrile oxides by modificatin of dipolarophiles
    Kamimura, A.; Hori, K.
    Tetrahedron
    1994, 50, 7969–7980. http://dx.doi.org/
  123. Reversing the Regiochemical Course of 1,3-Dipolar Cycloaddition of Nitrile oxides by Modification of Dipolarophiles
    Kamimura, A.; Hori, K.
    Tetrahedron
    1994, 50, 7979–7980. http://dx.doi.org/10.1016/S0040-4020(01)85282-0
  124. An experimental and theoretical study on stereoselective addition to 3-formyl-Δ2-isoxazolines. Part 1. 1,3-anti-selectivity induced by BF3·OEt2
    Kamimura, A.; Kakehi, A.; Hori, K.
    Tetrahedron
    1993, 49, 7637–7648. http://dx.doi.org/10.1016/S0040-4020(01)87239-2
  125. Theoretical study on crown compounds as building blocks of functional molecules I. The relation between the hole size and the number of atoms in the ring of cyclic ethers and amines
    Hori, K.; Haruna, Y.; Kamimura, A.; Tsukube, H.; Inoue, T.
    Tetrahedron
    1993, 49, 3959–3970. http://dx.doi.org/10.1016/S0040-4020(01)89910-5
  126. Novel tellurium‐containing p‐terphenoquinone analogues: Preparation and unique redox properties of paramagnetic tellurium‐centered radical cation complexes
    Tamura, R.; Nagata, Y.; Matsumoto, A.; Shimizu, H.; Ono, N.; Kamimura, A.; Hori, K.
    Adv. Mater.
    1993, 5, 719–721. http://dx.doi.org/10.1002/adma.19930051005
  127. Lewis Acid Promoted Stereoselective Carbon-Carbon Bond Formation of 3-Formyl-Δ2-isoxazolines
    Kamimura, A.; Yoshihara, K.; Marumo, S.; Yamamoto, A.; Nishiguchi, T.; Hori, K.; Kakehi, A.
    J. Org. Chem.
    1992, 57, 5403–5413. http://dx.doi.org/10.1021/jo00046a023
  128. Stereoselective Synthesis of Cis 2,3-Disubstituted Cycloheptanones by Kinetic Protonation
    Tamura, R.; Watabe, K.-I.; Kamimura, A.; Hori, K.; Yokomori, Y.
    J. Org. Chem.
    1992, 57, 4903–4905. http://dx.doi.org/10.1021/jo00044a027
  129. Synthesis of Photolabile Caged Amino Acids for Measuring Amino Acid Transporters
    Aoshima, H.; Tanaka, D.; Kamimura, A.
    Biosci. Biotech. Biochem.
    1992, 56, 1086–1089. http://dx.doi.org/10.1271/bbb.56.1086
  130. Diastereoselective Cyclocondensation Reaction of 3-Formyl-2-isoxazolines
    Kamimura, A.; Kakehi, A.
    Chem. Lett. 1992, 1133–1136. https://doi.org/10.1246/cl.1992.1133
  131. 2−イソオキサゾリンの化学の最近の進歩―選択性の観点から
    上村明男
    有機合成化学協会誌 1992, 50, 808–825.
  132. Displacement of Aliphatic Nitro Groups by Carbon and Heteroatom Nucleophiles
    Tamura, R.;, Kamimura, A.; Ono, N.
    Synthesis 1991, 423–434. http://dx.doi.org/10.1055/s-1991-26484
  133. syn- and anti-Selective preparation of 3-substltuted-Δ2-isoxazolines
    Kamimura, A.; Marumo, S.
    Tetrahedron Lett.
    1990, 31, 5053–5056. http://dx.doi.org/10.1016/S0040-4039(00)97804-3
  134. Theoretical and Experimental Study on The Stereoselectivity of Michael Addition of Alkoxide Anion to Nitro Olefin
    Hori, K.; Higuchi, S.; Kamimura, A.
    J. Org. Chem.
    1990, 55, 5900–5905. http://dx.doi.org/10.1021/jo00310a024
  135. Anti-Selective Michael Addition of Thiols and Their Analogues to Nitro Olefins
    Kamimura, A.; Hori, K.; Sasatani, H.; Hashimoto, T.; Kawai, T.; Ono, N.
    J. Org. Chem.
    1990, 55, 2437–2442. http://dx.doi.org/10.1021/jo00295a036
  136. Ready Preparation of α-Nitroaldehyde Acetals from (E/Z)-1-Phenylthio-2-nitro-1-alkenes
    Kamimura, A.; Nagashima, T.
    Synthesis 1990, 694. http://dx.doi.org/10.1055/s-1990-26984
  137. Diastereoselective Ene Reaction of 3-Formyl-Δ2-isoxazolines
    Kamimura, A.; Yamamoto, A.
    Chem. Lett. 1990, 1991–1994. https://doi.org/10.1246/cl.1990.1991
  138. Lewis Acid Induced Nucleophilic Substitution Reaction of β-Nitro Sulfides
    Kamimura, A.; Sasatani, H.; Hashimoto, T.; Ono, N.
    J. Org. Chem.
    1989, 54, 4998–5003. http://dx.doi.org/10.1021/jo00282a009
  139. Diastereoselective preparation of anti-β-amino alcohols via michael addition of alkoxide anions to nitroolefins and subsequent hydrogenation reaction
    Kamimura, A.; Ono, N.
    Tetrahedron Lett.
    1989, 30, 731–734. http://dx.doi.org/10.1016/S0040-4039(01)80295-1
  140. A novel procedure for denitrohydrogenation by Na2S2O4-Et3SiH
    Kamimura, A.; Kurata, K.; Ono, N.
    Tetrahedron Lett.
    1989, 30, 4819–4820. http://dx.doi.org/10.1016/S0040-4039(01)80517-7
  141. Regioselective Preparation of Cyclohexadienes or Aromatic Nitro Compounds by Diels-Alder Reactions of β-Sulfonylnitroolefins or β-Sulfinylnitroethylene
    Ono, N.; Kamimura, A.; Kaji, A.
    J. Org. Chem.
    1988, 53, 251–258. http://dx.doi.org/10.1021/jo00237a005
  142. Stereoselective preparation of (E)-allyl alcohols via radical elimination from anti-γ-phenylthio-β-nitro alcohols
    Kamimura, A.; Ono, N.
    J. Chem. Soc., Chem. Commun.
    1988, 1278–1280. http://dx.doi.org/10.1039/C39880001278
  143. A Facile Method for Preparation of Nitroenamines
    Kamimura, A.; Ono, N.
    Synthesis 1988, 921–922. http://dx.doi.org/10.1055/s-1988-27757
  144. On the Mechanism of Reductive Cleavage of the Carbon-Nitrogen Bond of Aliphatic Nitro Copmpounds with Tributyltin Hydride
    Kamimura, A.; Ono, N.
    Bull. Chem. Soc. Jpn. 1988, 61, 3629–3635. https://doi.org/10.1246/bcsj.61.3629
  145. A convenient procedure for the conversion of (E)-nitroalkenes to (Z)-nitroalkenes via erythro-β-nitroselenides
    Ono, N.; Kamimura, A.; Kawai, T.; Kaji, A.
    J. Chem. Soc., Chem. Commun.
    1987, 1550–1551. http://dx.doi.org/10.1039/C39870001550
  146. Regioselective Diels-Alder reactions. The nitro group as a regiochemical control element
    Ono, N.; Miyake, H.; Kamimura, A.; Kaji, A.
    J. Chem. Soc., Perkin Trans. 1
    1987, 1929–1935. http://dx.doi.org/
  147. Stereospecific Anti Radical Elimination Reaction from β-Nitro Sulfones
    Ono, N.; Kamimura, A.; Kaji, A.
    J. Org. Chem.
    1987, 52, 5111–5116. http://dx.doi.org/10.1021/jo00232a010
  148. Lewis Acid Induced Nucleophilic Substitution Reactions of β-nitro Sulfides Via Episulfonium Ions
    Ono, N.; Kamimura, A.; Sasatani, H.; Kaji, A.
    J. Org. Chem.
    1987, 52, 4133–4135. http://dx.doi.org/10.1021/jo00227a039
  149. β–ニトロスルフィドの還元脱離反応によるオレフィン合成
    小野昇, 上村明男, 川合修次, 加治有恒
    日本化学会誌 1987, 1338–1345.
  150. Reaction of Carbanions Derived from α,β-Unsaturated Nitro Compounds with Electrophiles to Give α-Substituted Products
    Ono, N.; Hamamoto, I.; Kamimura, A.; Kaji, A.; and Tamura, R.
    Synthesis 1987, 258–260. http://dx.doi.org/10.1055/s-1987-27907
  151. β-Sulfonylnitroolefins as very reactive alkyne-equivalents in Diels-Alder reactions
    Ono, N.; Kamimura, A.; Kaji, A.
    Tetrahedron Lett.
    1986, 27, 1595–1598. http://dx.doi.org/10.1016/S0040-4039(00)84323-3
  152. Lewis acid-induced nucleophilic substitution reactions of aliphatic nitro compounds with carbon nucleophiles
    Ono, N.; Yanai, T.; Kamimura, A.; Kaji, A.
    J. Chem. Soc., Chem. Commun.
    1986, 1285–1287. http://dx.doi.org/10.1039/C39860001285
  153. Preparation of a New Type of Electron-Deficient Olefins: β-Phenylthio Nitro Olefins, β-Sulfinyl Nitro Olefins, and β-Sulfonyl Nitro Olefins
    Ono, N.; Kamimura, A.; Kaji, A.
    J. Org. Chem.
    1986, 51, 2139–2142. http://dx.doi.org/10.1021/jo00361a044
  154. Regioselective Removal of Allylic Nitro Groups via Hydride Transfer
    One, N.; Hamamoto, I.; Kamimura, A.; Kaji, A.
    J. Org. Chem.
    1986, 51, 3734–3736. http://dx.doi.org/10.1021/jo00369a043
  155. New Synthetic Methods. Conjugate Addition of Alkyl Groups to Electron Deficient Olefins with Nitroalkanes as Alkyl Anion Equivalents
    Ono, N.; Kamimura, A.; Miyake, H.; Hamamoto, I.; Kaji, A.
    J. Org. Chem.
    1985, 50, 3692–3698. http://dx.doi.org/10.1021/jo00220a003
  156. Nitro Compounds as Nucleophilic Alkylidene Transfer Reagents
    Ono, N.; Yanai, T.; Hamamoto, I.; Kamimura, A.; Kaji, A.
    J. Org. Chem.
    1985, 50, 2806–2807. http://dx.doi.org/10.1021/jo00215a052
  157. Denitrohydrogenation of aliphatic nitro compounds and a new use of aliphatic nitro compounds as radical precursors
    Ono, N.; Miyake, H.; Kamimura, A.; Hamamoto, I.; Tamura, R.; Kaji, A.
    Tetrahedron
    1985, 41, 4013–4023. http://dx.doi.org/10.1016/S0040-4020(01)97180-7
  158. Michael Addition of Secondary Nitroalkanes to β-Substituted α,β-Unsaturated Compounds.
    Ono, N.; Kamimura, A.; Kaji, A.;
    Synthesis 1984, 226–228. http://dx.doi.org/10.1055/s-1984-30780
  159. A new synthesis of allylic alcohols or their derivatives via reductive elimination from γ-phenylthio-β-nitroalcohols with tributyltinhydride
    Ono, N.; Kamimura, A.; Kaji, A.
    Tetrahedron Lett.
    1984, 25, 5319–5322. http://dx.doi.org/10.1016/S0040-4039(01)81593-8
  160. Conjugate addition of alkyl groups to α,β-unsaturated sulfoxides via Michael addition of nitroparaffins and subsequent denitration with tributyltin hydride
    Ono, N.; Miyake, H.; Kamimura, A.; Tsukui, N.; Kaji, A.
    Tetrahedron Lett.
    1982, 23, 2957–2960. http://dx.doi.org/10.1016/S0040-4039(00)87505-X

【books】

  1. [2 + 1]-type cyclopropanation reactions, in Methods and applications of cycloaddition reactions in organic syntheses, Ed. by Nagatoshi Nishiwaki, John Wiley and Sons, New Jersey, 2014 (pp 1 – 66).
  2. 化学は楽しいワンダーランド」単著 (丸善)
  3. 「実験化学講座 15巻 有機化合物の合成」分担執筆(丸善)
  4. 「有機合成のナビゲーター」単著 (丸善)
  5. 「初めての有機スペクトル解析」築部浩・宇野英満編 分担執筆(丸善)
  6. 「研究室で役立つ有機実験のナビゲーター」訳著(丸善)
  7. 「有機化学」奥山格著(丸善) 分担執筆
  8. 「研究室ですぐに使える有機合成のレシピ」訳著(丸善)
  9. 「各種手法による有機物の分解技術」分担執筆(情報機構)
  10. 「イオン液体IIIーナノ・バイオサイエンスへの挑戦ー」大野弘幸監修 分担執筆(シーエムシー出版)
  11. 「最先端材料システムOne Point2 イオン液体」高分子学会編集 分担執筆(共立出版)
  12. 「イオン液体の科学-新世代液体への挑戦-」イオン液体研究会 監督 西川恵子・大内幸雄・伊藤敏幸・大野弘幸・渡邊正義 編 分担執筆(丸善出版)
  13. 「新しい溶媒を用いた有機合成」分担執筆(S&T出版)
  14. 「フローチャートで考える有機反応機構」訳著(丸善出版)