{"id":38,"date":"2021-11-24T11:09:41","date_gmt":"2021-11-24T02:09:41","guid":{"rendered":"http:\/\/achem.okayama-u.ac.jp\/bioorgchem\/WordPress\/?page_id=38"},"modified":"2024-01-25T17:15:18","modified_gmt":"2024-01-25T08:15:18","slug":"member%ef%bc%88as%ef%bc%89","status":"publish","type":"page","link":"http:\/\/achem.okayama-u.ac.jp\/bioorgchem\/member%ef%bc%88as%ef%bc%89","title":{"rendered":"Member\uff08AS\uff09"},"content":{"rendered":"\n

\u5742\u5009\u3000\u5f70\u3000\uff08SAKAKURA Akira\uff09<\/strong><\/p>\n\n\n\n

\"\"<\/figure>\n\n\n\n

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TEL&FAX: \u00a0086-251-8215\u00a0
E-mail: \u00a0sakakura\uff20okayama-u.ac.jp\u00a0
ORCID:\u00a00000-0002-2995-1251\u00a0<\/a>
ResearcherID:\u00a0A-6319-2013\u00a0<\/a><\/p>\n\n\n\n

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1995\u5e74\u3000\u540d\u53e4\u5c4b\u5927\u5b66\u5927\u5b66\u9662\u7406\u5b66\u7814\u7a76\u79d1\u5316\u5b66\u5c02\u653b\u535a\u58eb\u524d\u671f\u8ab2\u7a0b\u4fee\u4e86\uff08\u5c71\u7530\u975c\u4e4b\u6559\u6388\uff09
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2001\u5e74\u3000\u7b51\u6ce2\u5927\u5b66\u5316\u5b66\u7cfb\u3000\u52a9\u624b\uff08\u6728\u8d8a\u82f1\u592b\u6559\u6388\uff09
2003\u5e74\u3000\u540d\u53e4\u5c4b\u5927\u5b66\u5927\u5b66\u9662\u5de5\u5b66\u7814\u7a76\u79d1\u3000\u8b1b\u5e2b\uff08\u77f3\u539f\u4e00\u5f70\u6559\u6388\uff09
2007\u5e74\u3000\u540d\u53e4\u5c4b\u5927\u5b66\u30a8\u30b3\u30c8\u30d4\u30a2\u79d1\u5b66\u7814\u7a76\u6240\u3000\u51c6\u6559\u6388\uff08\u77f3\u539f\u4e00\u5f70\u6559\u6388\uff09
2012\u5e74\u3000\u5ca1\u5c71\u5927\u5b66\u5927\u5b66\u9662\u81ea\u7136\u79d1\u5b66\u7814\u7a76\u79d1\uff08\u5de5\u5b66\u7cfb\uff09\u3000\u6559\u6388<\/p>\n\n\n\n

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1. \u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u6771\u6d77\u652f\u90e8\u5968\u52b1\u8cde (2005\u5e74)
\u3000\u300c\u751f\u7269\u6d3b\u6027\u7269\u8cea\u3092\u6307\u5411\u3057\u305f\u4f4e\u74b0\u5883\u8ca0\u8377\u578b\u89e6\u5a92\u7684\u8131\u6c34\u7e2e\u5408\u53cd\u5fdc\u306e\u958b\u62d3\u300d
2. \u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u3000\u842c\u6709\u88fd\u85ac\u7814\u7a76\u4f01\u753b\u8cde (2006\u5e74)
\u3000\u300c\u6c42\u6838\u89e6\u5a92\u306b\u3088\u308b\u4e0d\u6589\u30cf\u30ed\u30b2\u30f3\u5316\u3092\u5229\u7528\u3057\u305f\u542b\u30cf\u30ed\u30b2\u30f3\u74b0\u72b6\u5316\u5408\u7269\u306e\u30a8\u30ca\u30f3\u30c1\u30aa\u9078\u629e\u7684\u5408\u6210\u6cd5\u306e\u958b\u62d3\u300d
3. \u65e5\u672c\u5316\u5b66\u4f1a\u7b2c86\u6625\u5b63\u5e74\u4f1a\u3000\u82e5\u3044\u4e16\u4ee3\u306e\u7279\u5225\u8b1b\u6f14\u8cde (2006\u5e74)
\u3000\u300c\u751f\u7269\u6d3b\u6027\u7269\u8cea\u5408\u6210\u3092\u6307\u5411\u3057\u305f\u74b0\u5883\u4f4e\u8ca0\u8377\u8131\u6c34\u7e2e\u5408\u53cd\u5fdc\u306e\u958b\u62d3\u300d
4. Thieme Chemistry Journal Award (2006\u5e74)
\u3000the editorial boards of Synlett and Synthesis, Thieme Chemistry in Thieme Publishing Group
5. \u6709\u6a5f\u5408\u6210\u5316\u5b66\u5968\u52b1\u8cde (2008\u5e74)
\u3000\u300c\u9178\u30fb\u5869\u57fa\u8907\u5408\u5869\u3092\u9375\u3068\u3059\u308b\u9ad8\u6a5f\u80fd\u89e6\u5a92\u306e\u8a2d\u8a08\u53ca\u3073\u9ad8\u9078\u629e\u7684\u5408\u6210\u6cd5\u306e\u958b\u62d3\u300d
6. Banyu Chemist Award (2009\u5e74)
\u3000\u300c\u9178\u30fb\u5869\u57fa\u8907\u5408\u5869\u578b\u89e6\u5a92\u306e\u7cbe\u5bc6\u8a2d\u8a08\u3092\u57fa\u76e4\u3068\u3057\u305f\u9ad8\u9078\u629e\u7684\u5408\u6210\u6cd5\u306e\u958b\u62d3\u300d
\u3000\u201cDevelopment of Highly Selective Reactions Based on Rational Design of Acid-Base Combined Salt Catalysts\u201d
7. Asian Core Program Lectureship Award (2010\u5e74)
\u3000\u201cDesign of Bronsted Base-Assisted Boronic Acid Catalysis for the Dehydrative Intramolecular Condensation of Dicarboxylic Acids\u201d
\u3000The 5th International Conference on Cutting-Edge Organic Chemistry in Asia (ICCEOCA-5)<\/p>\n\n\n\n

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\u767a\u8868\u8ad6\u6587<\/h4>\n\n\n\n

1. \"Synthetic Studies on Aplyronine A, a Potent Antitumor Substance of Marine Origin: Stereocontrolled Synthesis of the C21\u2013C34 Segment\"
Hideo Kigoshi, Makoto Ojika, Kiyotake Suenaga, Tsuyoshi Mutou, Junko Hirano, Akira Sakakura, Takeshi Ogawa, Masanori Nisiwaki, Kiyoyuki Yamada,* Tetrahedron Lett.<\/em> 1994<\/strong>, 35<\/em>, 1247\u20131250.  
DOI: 10.1016\/0040-4039(94)88035-2 <\/a>
 
2. \"Total Synthesis of Aplyronine A, a Potent Antitumor Substance of Marine Origin\"
Hideo Kigoshi, Makoto Ojika, Takeshi Ishigaki, Kiyotake Suenaga, Tsuyoshi Mutou, Akira Sakakura, Takeshi Ogawa, Kiyoyuki Yamada,* J. Am. Chem. Soc.<\/em> 1994<\/strong>, 116<\/em>, 7443\u20137444.  
DOI: 10.1021\/ja00095a072 <\/a>
 
3. \"Absolute Stereochemistry and Synthesis of Aplyronines B and C, the Congeners of Aplyronine A, a Potent Antitumor Substance of Marine Origin\"
Kiyotake Suenaga, Takeshi Ishigaki, Akira Sakakura, Hideo Kigoshi, Kiyoyuki Yamada,* Tetrahedron Lett.<\/em> 1995<\/strong>, 36<\/em>, 5053\u20135056.  
DOI: 10.1016\/0040-4039(95)00921-X <\/a>
 
4. \"Aplyronine A, a Potent Antitumor Substance of Marine Origin, Aplyronines B and C, and Artificial Analogues: Total Synthesis and Structure\u2013Cytotoxicity Relationships\"
Hideo Kigoshi, Kiyotake Suenaga, Tsuyoshi Mutou, Takeshi Ishigaki, Toshiyuki Atsumi, Hiroyuki Ishiwata, Akira Sakakura, Takeshi Ogawa, Makoto Ojika, Kiyoyuki Yamada,* J. Org. Chem.<\/em> 1996<\/strong>, 61<\/em>, 5326\u20135351.  
DOI: 10.1021\/jo9606113 <\/a>
 
5. \"A Novel Approach to Oligodeoxyribonucleotides Bearing Phosphoric Acid Esters at the 3\u2019-Terminals via the Phosphoramidite Method with Allyl Protection: an Efficient Synthesis of Base-Labile Nucleotide\u2013Amino Acid and \u2013Peptide Conjugates\"
Akira Sakakura, Yoshihiro Hayakawa,* Hitoshi Harada, Masaaki Hirose, Ryoji Noyori,* Tetrahedron Lett.<\/em> 1999<\/strong>, 40<\/em>, 4359\u20134362.  
DOI: 10.1016\/S0040-4039(99)00748-0 <\/a>
 
6. \"A Novel Synthesis of Oligonucleotide\u2013Peptide Conjugates with a Base-Labile Phosphate Linker between the Two Components According to the Allyl-Protected Phosphoramidite Strategy\"
Akira Sakakura, Yoshihiro Hayakawa,* Tetrahedron<\/em> 2000<\/strong>, 56<\/em>, 4427\u20134435.  
DOI: 10.1016\/S0040-4020(00)00376-8 <\/a>
 
7. \"A Facile Synthesis of 5\u2019-End Solid-Anchored, 3\u2019-End Free Oligodeoxyribonucleotides via the (5\u2019\u21923\u2019)-Elongated Phosphoramidite Strategy\"
Akira Sakakura, Yoshihiro Hayakawa,* Nucleosides, Nucleotides, Nucleic Acids<\/em> 2001<\/strong>, 20<\/em>, 213\u2013227.  
DOI: 10.1081\/NCN-100002082 <\/a>
 
8. \"Acid\/Azole Complexes as Highly Effective Promoters in the Synthesis of DNA and RNA Oligomers via the Phosphoramidite Method\"
Yoshihiro Hayakawa,* Rie Kawai, Akiyoshi Hirata, Jun-ichiro Sugimoto, Masanori Kataoka, Akira Sakakura, Masaaki Hirose, and Ryoji Noyori, J. Am. Chem. Soc.<\/em> 2001<\/strong>, 123<\/em>, 8165\u20138176.  
DOI: 10.1021\/ja010078v <\/a>
 
9. \"Effect of Molecular Sieves in the Liquid-Phase Synthesis of Nucleotides via the Phosphoramidite Method\"
Yoshihiro Hayakawa,* Akiyoshi Hirata, Jun-ichiro Sugimoto, Rie Kawai, Akira Sakakura, Masanori Kataoka, Tetrahedron<\/em> 2001<\/strong>, 57<\/em>, 8823\u20138826.  
DOI: 10.1016\/S0040-4020(01)00880-8 <\/a>
 
10. \"Jolkinolide D Pharmacophore: Synthesis and Reaction with Amino Acids, Nucleosides, and DNA\"
Akira Sakakura, Yui Takayanagi, Hideo Kigoshi,* Tetrahedron Lett.<\/em> 2002<\/strong>, 43<\/em>, 6055\u20136058.  
DOI: 10.1016\/S0040-4039(02)01195-4 <\/a>
 
11. \"Nonspecificity Induces Chiral Specificity in the Folding Transition of Giant DNA\"
Michiko Ito, Akira Sakakura, Naomi Miyazawa, Shizuaki Murata,* Kenichi Yoshikawa, J. Am. Chem. Soc.<\/em> 2003<\/strong>, 125<\/em>, 12714\u201312715.  
DOI: 10.1021\/ja036745x <\/a>
 
12. \"Jolkinolide D Pharmacophore: Synthesis and Reaction with Biomolecules\"
Akira Sakakura, Yui Takayanagi, Hiroki Shimogawa, Hideo Kigoshi,* Tetrahedron<\/em> 2004<\/strong>, 60<\/em>, 7067\u20137075.  
DOI: 10.1016\/j.tet.2003.08.080 <\/a>
 
13. \"Synthesis and actin-depolymerizing activity of mycalolide analogs\"
Kiyotake Suenaga, Saori Miya, Takeshi Kuroda, Tomohisa Handa, Kengo Kanematsu, Akira Sakakura, Hideo Kigoshi,* Tetrahedron Lett.<\/em> 2004<\/strong>, 45<\/em>, 5383\u20135386.  
DOI: 10.1016\/j.tetlet.2004.05.078 <\/a>
 
14. \"Spongiacysteine, a Novel Cysteine Derivative from Marine Sponge Spingia sp.\"
Keiko Kobayashi, Hiroki Shimogawa, Akira Sakakura, Toshiaki Teruya, Kiyotake Suenaga, Hideo Kigoshi,* Chem. Lett.<\/em> 2004<\/strong>, 33<\/em>, 1262\u20131263.  
DOI: 10.1246\/cl.2004.1262 <\/a>
 
15. \"Formal Synthesis of Optically Active Ingenol via Ring-Closing Olefin Methathesis\"
Kazushi Watanabe, Yuto Suzuki, Kenta Aoki, Akira Sakakura, Kiyotake Suenaga, Hideo Kigoshi,* J. Org. Chem.<\/em> 2004<\/strong>, 69<\/em>, 7802\u20137808.  
DOI: 10.1021\/jo048833l <\/a>
 
16. \"Bulky Diarylammonium Arenesulfonates as Selective Esterification Catalysts\"
Kazuaki Ishihara,* Shoko Nakagawa, Akira Sakakura, J. Am. Chem. Soc.<\/em> 2005<\/strong>, 127<\/em>, 4168\u20134169.  
DOI: 10.1021\/ja050223v <\/a>
 
17. \"Molybdenum Oxides as Highly Effective Dehydrative Cyclization Catalysts for the Synthesis of Oxazolines and Thiazolines\"
Akira Sakakura, Rei Kondo, Kazuaki Ishihara,* Org. Lett.<\/em> 2005<\/strong>, 7<\/em>, 1971\u20131974.  
DOI: 10.1021\/ol050543j <\/a>
 
18. \"Selective Synthesis of Phosphate Monoesters by Dehydrative Condensation of Phosphoric Acid and Alcohols Promoted by Nucleophilic Bases\"
Akira Sakakura, Mikimoto Katsukawa, Kazuaki Ishihara,* Org. Lett.<\/em> 2005<\/strong>, 7<\/em>, 1999\u20132002.  
DOI: 10.1021\/ol0504796 <\/a>
 
19. \"Bulky diarylammonium arenesulfonates as mild and extremely active dehydrative ester condensation catalysts\"
Akira Sakakura, Shoko Nakagawa, Kazuaki Ishihara,* Tetrahedron<\/em> 2006<\/strong>, 62<\/em>, 422\u2013433.  
DOI: 10.1016\/j.tet.2005.09.059 <\/a>
 
20. \"Study of the Interaction between Actin and Antitumor Substance Aplyronine A with a Novel Fluorescent Photoaffinity Probe\"
Takeshi Kuroda, Kiyotake Suenaga, Akira Sakakura, Tomohisa Handa, Kazuhito Okamoto, Hideo Kigoshi,* Bioconjugate Chem.<\/em> 2006<\/strong>, 17<\/em>, 524\u2013529.  
DOI: 10.1021\/bc050324i <\/a>
 
21. \"Chiral 1,1'-Binaphthyl-2,2'-diammonium Salt Catalysts for the Enantioselective Diels\u2013Alder Reaction with \u03b1-Acyloxyacroleins\"
Akira Sakakura, Kenji Suzuki, Kazuhiko Nakano, Kazuaki Ishihara,* Org. Lett.<\/em> 2006<\/strong>, 8<\/em>, 2229\u22122232.  
DOI: 10.1021\/ol060490l <\/a>
 
22. \"Enantioselective Diels\u2013Alder Reaction of \u03b1-Acyloxyacroleins Catalyzed by Chiral 1,1'-Binaphthyl-2,2'-diammonium Salts\"
Akira Sakakura, Kenji Suzuki, Kazuaki Ishihara,* Adv. Synth. Catal.<\/em> 2006<\/strong>, 348<\/em>, 2457\u20132465.  
DOI: 10.1002\/adsc.200600322 <\/a>
 
23. \"Enantioselective synthesis of aurisides A and B, cytotoxic macrolide glycosides of marine origin\"
Kiyotake Suenaga, Hiroshi Hoshino, Takanori Yoshii, Kazunori Mori, Hiroki Sone, Yuhki Bessho, Akira Sakakura, Ichiro Hayakawa, Kiyoyuki Yamada, Hideo Kigoshi,* Tetrahedron<\/em> 2006<\/strong>, 62<\/em>, 7687\u20137698.  
DOI: 10.1016\/j.tet.2006.05.077 <\/a>
 
24. \"Synthesis and biological activity of mycalolide analogs\"
Kiyotake Suenaga,* Tomoyuki Kimura, Takeshi Kuroda, Keita Matsui, Saori Miya, Satomi Kuribayashi, Akira Sakakura, Hideo Kigoshi,* Tetrahedron<\/em>2006<\/strong>, 62<\/em>, 8278\u20138290.  
DOI: 10.1016\/j.tet.2006.06.046 <\/a>
 
25. \"The Oxorhenium(VII)-Catalyzed Direct Condensation of Phosphoric Acid with an Alcohol\"
Akira Sakakura, Mikimoto Katsukawa, Kazuaki Ishihara,* Angew. Chem. Int. Ed.<\/em> 2007<\/strong>, 46<\/em>, 1423\u20131426.  
DOI: 10.1002\/anie.200604333 <\/a>
 
26. \"Enantioselective halocyclization of polyprenoids induced by nucleophilic phosphoramidites\"
Akira Sakakura, Atsushi Ukai, Kazuaki Ishihara,* Nature<\/em> 2007<\/strong>, 455<\/em>, 900\u2013903.  
DOI: 10.1038\/nature05553 <\/a>
 
27. \"Dehydrative Cyclization Catalyzed by the Combination of Molybdenum(VI) Oxides and Benzoic Acids: First Synthesis of the Antitumor Substance BE-70016\"
Akira Sakakura, Shuhei Umemura, Rei Kondo, Kazuaki Ishihara,* Adv. Synth. Catal.<\/em> 2007<\/strong>, 349<\/em>, 551\u2013555.  
DOI: 10.1002\/adsc.200600550 <\/a>
 
28. \"Unusual Rate-Acceleration in the Br\u00f8nsted Acid-Catalyzed Dehydration Reactions: Local Hydrophobic Environment in Aggregated N<\/em>-(2,6-Diphenylphenyl)-N<\/em>-mesitylammonium Pentafluorobenzenesulfonates\"
Akira Sakakura, Hitoshi Watanabe, Shoko Nakagawa, Kazuaki Ishihara,* Chem. Asian J.<\/em> 2007<\/strong>, 2<\/em>, 477\u2013483.  
DOI: 10.1002\/asia.200600380 <\/a>
 
29. \"Catalytic Synthesis of Peptide-Derived Thiazolines and Oxazolines Using Bis(quinolinolato)dioxomolybdenum(VI) Complexes\"
Akira Sakakura, Rei Kondo, Shuhei Umemura, Kazuaki Ishihara,* Adv. Synth. Catal.<\/em> 2007<\/strong>, 349<\/em>, 1641\u20131646.  
DOI: 10.1002\/adsc.200700068 <\/a>
 
30. \"Direct ester condensation catalyzed by bulky diarylammonium pentafluorobenzenesulfonates\"
Akira Sakakura, Shoko Nakagawa, Kazuaki Ishihara,* Nature Protocols<\/em> 2007<\/strong>, 2<\/em>, 1746\u20131751.  
DOI: 10.1038\/nprot.2007.254 <\/a>
 
31. \"Bulky phosphazenium cation catalysis for dehydrative condensation of phosphoric acid with alcohols\"
Akira Sakakura, Mikimoto Katsukawa, Takaomi Hayashi, Kazuaki Ishihara,* Green Chem.<\/em> 2007<\/strong>, 9<\/em>, 1166\u20131169.
DOI: 10.1039\/B707974E <\/a>
 
32. \"Widely Useful DMAP-Catalyzed Esterification under Auxiliary Base- and Solvent-Free Conditions\"
Akira Sakakura, Kimio Kawajiri, Takuro Ohkubo, Yuji Kosugi, Kazuaki Ishihara,* J. Am. Chem. Soc.<\/em> 2007<\/strong>, 129<\/em>, 14775\u201314779.
DOI: 10.1021\/ja075824w <\/a>
 
33. \"Selective Synthesis of Cyclic Phosphoric Acid Diesters Through Oxorhenium(VII)-Catalyzed Dehydrative Condensation of Phosphoric Acid with Alcohols\"
Akira Sakakura, Masayuki Sakuma, Mikimoto Katsukawa, Kazuaki Ishihara,* Heterocycles<\/em> 2008<\/strong>, 76<\/em>, 657\u2013665.
DOI: 10.3987\/COM-08-S(N)58 <\/a>
 
34. \"Convergent Total Syntheses of Fluvibactin and Vibriobactin Using Molybdenum(VI) Oxide-Catalyzed Dehydrative Cyclization as a Key Step\"
Akira Sakakura, Shuhei Umemura, Kazuaki Ishihara,* Chem. Commun.<\/em> 2008<\/strong>, 3561\u20133563.
DOI: 10.1039\/B805880F <\/a>
 
35. \"Rate-Accelerating Effect by the Neighboring-Group Participation of Protecting Groups in the Dehydrative Cyclization of 1,3,5-Triketones\"
Akira Sakakura, Hitoshi Watanabe, Kazuaki Ishihara,* Org. Lett.<\/em> 2008<\/strong>, 10<\/em>, 2569\u20132572.
DOI: 10.1021\/ol800860p <\/a>
 
36. \"Kinetic Resolution of Racemic Carboxylic Acids by an L-Histidine-derived Sulfonamide-induced Enantioselective Esterification Reaction\"
Kazuaki Ishihara,* Yuji Kosugi, Shuhei Umemura, Akira Sakakura, Org. Lett.<\/em> 2008<\/strong>, 10<\/em>, 3191\u20133194.
DOI: 10.1021\/ol801007m <\/a>
 
37. \"Open-air and solvent-free ester condensation catalyzed by sulfuric acids\"
Akira Sakakura, Yoshiki Koshikari, Kazuaki Ishihara,* Tetrahedron Lett.<\/em> 2008<\/strong>, 49<\/em>, 5017\u20135020.
DOI: 10.1016\/j.tetlet.2008.06.058 <\/a>
 
38. \"Dehydrative cyclization of serine, threonine and cysteine residues catalyzed by molybdenum(VI) oxo compounds\"
Akira Sakakura, Rei Kondo, Shuhei Umemura, Kazuaki Ishihara,* Tetrahderon<\/em> 2009<\/strong>, 65<\/em>, 2102\u20132109.
DOI: 10.1016\/j.tet.2008.12.074 <\/a>
 
39. \"3-Pyrroline-1-carbonyl (Pyroc) Group: A Removable Protecting Group for the Kinetic Resolution of Racemic Carboxylic Acids and Alcohols through Catalytic Asymmetric Acylation\"
Akira Sakakura, Shuhei Umemura, Kazuaki Ishihara,* Synlett<\/em> 2009<\/strong>, 1647\u20131650.
DOI: 10.1055\/s-0029-1217321 <\/a>
 
40. \"Rational Design of Highly Effective Asymmetric Diels-Alder Catalysts Bearing 4,4\u2032-Sulfonamidomethyl Groups\"
Akira Sakakura, Rei Kondo, Yuki Matsumura, Matsujiro Akakura, Kazuaki Ishihara,* J. Am. Chem. Soc.<\/em> 2009<\/strong>, 131<\/em>, 17762\u201317764.
DOI: 10.1021\/ja906098b <\/a>
 
41. \"Nucleophilic Phosphine\u2013Catalyzed Iodocyclization of Isoprenoids Bearing an Oxygen Terminal Group\"
Akira Sakakura, Gakujun Shomi, Atsushi Ukai, Kazuaki Ishihara,* Heterocycles<\/em> 2010<\/strong>, 82<\/em>, 249\u2013255.
DOI: 10.3987\/COM-09-S(E)1 <\/a>
 
42. \"Catalytic Enantioselective 1,3-Dipolar Cycloadditions of Nitrones with Propioloylpyrazoles and Acryloylpyrazoles Induced by Chiral \u03c0\u2013Cation Catalysts\"
Akira Sakakura, Masahiro Hori, Makoto Fushimi, Kazuaki Ishihara,* J. Am. Chem. Soc.<\/em> 2010<\/strong>, 132<\/em>, 15550\u201315552.
DOI: 10.1021\/ja1081603 <\/a>
 
43. \"Br\u00f8nsted Base-Assisted Boronic Acid Catalysis for the Dehydrative Intramolecular Condensation of Dicarboxylic Acids\"
Akira Sakakura, Takuro Ohkubo, Risa Yamashita, Matsujiro Akakura, Kazuaki Ishihara,* Org. Lett.<\/em> 2011<\/strong>, 13<\/em>, 892\u2013895.
DOI: 10.1021\/ol102926n <\/a>
 
44. \"Chiral Lewis Base-Assisted Br\u00f8nsted Acid (LBBA)-Catalyzed Enantioselective Cyclization of 2-Geranylphenols\"
Akira Sakakura, Masayuki Sakuma, Kazuaki Ishihara,* Org. Lett.<\/em> 2011<\/strong>, 13<\/em>, 3130\u20133133.
DOI: 10.1021\/ol201032t <\/a>
 
45. \"Desymmetrization of Meso Glycerol Derivatives Induced by L-Histidine-Derived Acylation Catalysts\"
Akira Sakakura, Shuhei Umemura, Kazuaki Ishihara,* Adv. Synth. Catal.<\/em> 2011<\/strong>, 353<\/em>, 1938\u20131942.
DOI: 10.1002\/adsc.201100252 <\/a>
 
46. \"Intramolecular Dehydrative Condensation of Dicarboxylic Acids with Br\u00f8nsted Base-Assisted Boronic Acid Catalysts\"
Akira Sakakura, Risa Yamashita, Takuro Ohkubo, Matsujiro Akakura, Kazuaki Ishihara,* Aust. J. Chem.<\/em> 2011<\/strong>, 64<\/em>, 1458\u20131465.
DOI: 10.1071\/CH11301 <\/a>
 
47. \"Hydrophobic N,N<\/em>-Diarylammonium Pyrosulfates as Dehydrative Condensation Catalysts under Aqueous Conditions\"
Akira Sakakura, Yoshiki Koshikari, Matsujiro Akakura, Kazuaki Ishihara,* Org. Lett.<\/em> 2012<\/strong>, 14<\/em>, 30\u201333.
DOI: 10.1021\/ol2027366 <\/a>
 
48. \"Aplyronines D\u2013H from the sea hare Aplysia kurodai: isolation, structures, and cytotoxicity\"
Makoto Ojika,* Hideo Kigoshi, Kiyotake Suenaga, Yoshifumi Imamura, Kohji Yoshikawa, Takeshi Ishigaki, Akira Sakakura, Tsuyoshi Mutou, Kiyoyuki Yamada,* Tetrahedron<\/em> 2012<\/strong>, 68<\/em>, 982\u2013987.
DOI: 10.1016\/j.tet.2011.11.095 <\/a>
 
49. \"Enantioselective Diels\u2013Alder Reaction of \u03b1-(Acylthio)acroleins: a New Entry to Sulfur-containing Chiral Quaternary Carbons\"
Akira Sakakura, Hiroki Yamada, Kazuaki Ishihara,* Org. Lett.<\/em> 2012<\/strong>, 14<\/em>, 2972\u20132975.
DOI: 10.1021\/ol300921f <\/a>
 
50. \"N,N-Diarylammonium Pyrosulfate as a Highly Effective Reverse Micelle-type Catalyst for Hydrolysis of Esters\"
Yoshiki Koshikari, Akira Sakakura, Kazuaki Ishihara,* Org. Lett.<\/em> 2012<\/strong>, 14<\/em>, 3194\u20133197.
DOI: 10.1021\/ol301290c <\/a>
 
51. \"\u03b1-Heterosubstituted \u03b2-Alkylacroleins as Useful Multisubstituted Dienophiles for Enantioselective Diels-Alder Reactions\"
Akira Sakakura, Hiroki Yamada, Kazuaki Ishihara,* Asian J. Org. Chem.<\/em> 2012<\/strong>, 1<\/em>, 133\u2013137.
DOI: 10.1002\/ajoc.201200054 <\/a>
 
52. \"Kinetic Resolution of Racemic Carboxylic Acids through Asymmetric Protolactonization Promoted by Chiral Phosphonous Acid Diester\"
Masayuki Sakuma, Akira Sakakura,* Kazuaki Ishihara,* Org. Lett.<\/em> 2013<\/strong>, 15<\/em>, 2838\u20132841.
DOI: 10.1021\/ol401313d <\/a>
 
53. \"Primary Alkylboronic Acids as Highly Active Catalysts for the Dehydrative Amide Condensation of \u03b1-Hydroxycarboxylic Acids\"
Risa Yamashita, Akira Sakakura,* Kazuaki Ishihara,* Org. Lett.<\/em> 2013<\/strong>, 15<\/em>, 3654\u20133657.
DOI: 10.1021\/ol401537f <\/a>
 
54. \"Enantioselective Cyanoethoxycarbonylation of Isatins Promoted by a Lewis Base\u2013Br\u00f8nsted Acid Cooperative Catalyst\"
Yoshihiro Ogura, Matsujiro Akakura, Akira Sakakura,* Kazuaki Ishihara,* Angew. Chem. Int. Ed.<\/em> 2013<\/strong>, 52<\/em>, 8299\u20138303.
DOI: 10.1002\/anie.201303572 <\/a>
 
55. \"\u201cPhosphite\u2013Urea\u201d Cooperative High-Turnover Catalysts for the Highly Selective Bromocyclization of Homogeranylarenes\"
Yasuhiro Sawamura, Hidefumi Nakatsuji, Akira Sakakura,* Kazuaki Ishihara,* Chem. Sci.<\/em> 2013<\/strong>, 4<\/em>, 4181\u20134186.
DOI: 10.1039\/C3SC51432C <\/a>
 
56. \"Selective Bromocyclization of 2-Geranylphenols Promoted by Phosphite\u2013Urea Cooperative Catalysts\"
Yasuhiro Sawamura, Hidefumi Nakatsuji, Matsujiro Akakura, Akira Sakakura,* Kazuaki Ishihara,* Chirality<\/em> 2014<\/strong>, 26<\/em>, 356\u2013360.
DOI: 10.1002\/chir.22297 <\/a>
 
57. \"Catalytic Enantioselective Inverse Electron Demand Hetero-Diels\u2013Alder Reaction with Allylsilanes\"
Yuki Matsumura, Takahiro Suzuki, Akira Sakakura,* Kazuaki Ishihara,* Angew. Chem. Int. Ed.<\/em> 2014<\/strong>, 53<\/em>, 6131\u20136134.
DOI: 10.1002\/anie.201402934 <\/a>
 
58. \"Cooperative Activation with Chiral Nucleophilic Catalysts and N<\/em>-Haloimides: Enantioselective Iodolactonization of 4-Arylmethyl-4-pentenoic Acids\"
Hidefumi Nakatsuji, Yasuhiro Sawamura, Akira Sakakura,* Kazuaki Ishihara,* Angew. Chem. Int. Ed.<\/em> 2014<\/strong>, 53<\/em>, 6974\u20136977.
DOI: 10.1002\/anie.201400946 <\/a>
 
59. \"Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Imines with Propioloylpyrazoles Induced by Chiral \u03c0\u2212Cation Catalysts\"
Masahiro Hori, Akira Sakakura,* Kazuaki Ishihara,* J. Am. Chem. Soc.<\/em> 2014<\/strong>, 136<\/em>, 13198\u201313201.
DOI: 10.1021\/ja508441t <\/a>
 
60. \"Stereoselective Electrophilic Cyclization\"
Akira Sakakura,* Kazuaki Ishihara,* Chem. Rec.<\/em> 2015<\/strong>, 15<\/em>, 728\u2013742.
DOI: 10.1002\/tcr.201500005 <\/a>
 
61. \"Enantioselective Bromocyclization of 2-Gernaylphenols Induced by Chiral Phosphite-Urea Bifunctional Catalysts\"
Yasuhiro Sawamura, Yoshihiro Ogura, Hidefumi Nakatsuji, Akira Sakakura,* Kazuaki Ishihara,* Chem. Common.<\/em> 2016<\/strong>, 52<\/em>, 6068\u20136071.
DOI: 10.1039\/C6CC00229C <\/a>
 
62. \"A short access to 3,5-disubstituted piperazinones based on the aza-Michael addition of \u03b1-amino esters to \u03b2-substituted nitroalkenes\"
Takayuki Kudoh,* Seiji Isoyama, Sachiko Kagimoto, Katsutoshi Kurihara, Akira Sakakura,* Tetrahedron Lett.<\/em> 2016<\/strong>, 57<\/em>, 4693\u20134696.
DOI: 10.1016\/j.tetlet.2016.09.015 <\/a>
 
63. \"Discovery of O6-benzyl glaziovianin A, a potent cytotoxic substance and a potent inhibitor of \u03b1,\u03b2-tubulin polymerization\"
Ichiro Hayakawa,* Shuya Shioda, Takumi Chinen, Taisei Hatanaka, Haruna Ebisu, Akira Sakakura, Takeo Usui,* Hideo Kigoshi,* Bioorg. Med. Chem.<\/em>2016<\/strong>, 24<\/em>, 5639\u20135645.
DOI: 10.1016\/j.bmc.2016.09.026 <\/a>
 
64. \"Reinvestigation of the Biomimetic Cyclization of 3,5-Diketo Esters: Application to the Total Synthesis of Cyercene A, an \u03b1-Methoxy-\u03b3-Pyrone-Containing Polypropionate\"
Kai Onda, Ichiro Hayakawa, Akira Sakakura,* Synlett<\/em> 2017<\/strong>, 28<\/em>, 1596\u20131600.
DOI: 10.1055\/s-0036-1588795 <\/a>
 
65. \"Heat Versus Basic Conditions: Intramolecular Dehydro-Diels\u2013Alder Reaction of 1-Indolyl-1,6-heptadiynes for the Selective Synthesis of Substituted Carbazoles\"
Takayuki Kudoh, Syo Fujisawa, Megumi Kitamura, Akira Sakakura,* Synlett<\/em> 2017<\/strong>, 28<\/em>, 2189\u20132193.
DOI: 10.1055\/s-0036-1588461 <\/a>
 
66. \"Diastereodivergent Henry Reaction for the Stereoselective Construction of Nitrogen-Containing Tetrasubstituted Carbons: Application to Total Synthesis of Manzacidins A and C\"
Takayuki Kudoh, Yuya Araki, Natsumi Miyoshi, Mizuho Tanioka, Akira Sakakura,* Asian J. Org. Chem.<\/em> 2017<\/strong>, 6<\/em>, 1760\u20131763.
DOI: 10.1002\/ajoc.201700568 <\/a>
 
67. \"Regioselective DMAD-insertion reaction of silyl dienol ether of \u03b3-pyrone under catalyst- and heating-free conditions\"
Ichiro Hayakawa,* Yuji Yamanaka, Koichi Mitsudo, Hiromi Ota, Akira Sakakura,* Heterocycles<\/em> 2017<\/strong>, 94<\/em>, 2299\u20132306.
DOI: 10.3987\/COM-17-13820 <\/a>
 
68. \"Enantioselective Aza-Friedel\u2013Crafts Reaction of Furan with \u03b1-Ketimino Esters Induced by a Conjugated Double Hydrogen Bond Network of Chiral Bis(phosphoric Acid) Catalysts\"
Manabu Hatano, Haruka Okamoto, Taro Kawakami, Kohei Toh, Hidefumi Nakatsuji, Akira Sakakura,* Kazuaki Ishihara,* Chem. Sci.<\/em> 2018<\/strong>, 9<\/em> (30), 6361\u20136367.  
DOI: 10.1039\/C8SC02290A <\/a>
 
69. \"Chiral Pyrophosphoric Acid Catalysts for the para-Selective and Eanantioselective Aza-Friedel\u2013Crafts Reaction of Phenols\"
Haruka Okamoto, Kohei Toh, Takuya Mochizuki, Hidefumi Nakatsuji, Akira Sakakura,* Manabu Hatano,* Kazuaki Ishihara,* Synthesis<\/em> 2018<\/strong>, 50<\/em> (23), 4577\u20134590.  
DOI: 10.1055\/s-0037-1610250 <\/a>
 
70. \"Catalytic Enantioselective Hosomi\u2013Sakurai Reaction of \u03b1-Ketoesters Promoted by Chiral Copper(II) Complexes\"
Yutaro Niwa, Mayu Miyake, Ichiro Hayakawa, Akira Sakakura,* Chem. Commun.<\/em> 2019<\/strong>, 55<\/em> (27), 3923\u20133926.
DOI: 10.1039\/C9CC01159E <\/a>
 
71. \"Thioureas as Highly Active Catalysts for Biomimetic Bromocyclization of Geranyl Derivatives\"
Miyuki Terazaki, Kei-ichi Shiomoto, Haruki Mizoguchi, Akira Sakakura,* Org. Lett.<\/em> 2019<\/strong>, 21<\/em> (7), 2073\u20132076.
DOI: 10.1021\/acs.orglett.9b00352 <\/a>
 
72. \"Enantioselective 1,3-Dipolar Cycloaddition Reaction of Nitrones with \u03b1-(Acyloxy)acroleins Catalyzed by Dipeptide-Derived Chiral Tri- or Diammonium Salts\"
Chihiro Kidou, Haruki Mizoguchi, Tatsuo Nehira, Akira Sakakura,* Synlett <\/em>2019<\/strong>, 30<\/em> (15), 1835\u20131839.
DOI: 10.1055\/s-0039-1690133 <\/a>
 
73. \"Toward the Synthesis of Yuzurimine-type Alkaloids: Stereoselective Construction of the Heterocyclic Portions of Deoxyyuzurimine and Macrodaphnine\"
Ichiro Hayakawa,* Ryosuke Nagatani, Masaki Ikeda, Dong-eun Yoo, Keita Saito, Hideo Kigoshi, Akira Sakakura,* Org. Lett.<\/em> 2019<\/strong>, 21<\/em> (16), 6337\u20136341.
DOI: 10.1021\/acs.orglett.9b02232 <\/a>
 
74. \"Toward the Synthesis of SB-203207: Construction of Four Contiguous Nitrogen-Containing Stereogenic Centers\"
Ichiro Hayakawa,* Anna Nagayasu, Akira Sakakura,* J. Org. Chem.<\/em> 2019<\/strong>, 84<\/em> (23), 15614\u201315623.
DOI: 10.1021\/acs.joc.9b02627 <\/a>
 
75. \"Formal Total Synthesis of Manzacidin B via Sequential Diastereodivergent Henry Reaction\"
Yuya Araki, Natsumi Miyoshi, Kazuki Morimoto, Takayuki Kudoh, Haruki Mizoguchi, Akira Sakakura,* J. Org. Chem.<\/em> 2020<\/strong>, 85<\/em> (2), 798\u2013805.
DOI: 10.1021\/acs.joc.9b02811<\/a>
 
76. \"Structure Optimization of Gatastatin for the Development of \u03b3-Tubulin-Specific Inhibitor\"
Kana Shintani, Haruna Ebisu, Minagi Mukaiyama, Taisei Hatanaka, Takumi Chinen, Daisuke Takao, Yoko Nagumo, Akira Sakakura, Ichiro Hayakawa,* Takeo Usui,* ACS Med. Chem. Lett.<\/em> 2020<\/strong>, 11<\/em> (6), 1125\u20131129.
DOI: 10.1021\/acsmedchemlett.9b00526 <\/a>
 
77. \"Enantioselective Diels\u2013Alder Reaction of 3-Nitrocoumarins Promoted by Chiral Organoammonium Salt Catalysts\"
Yudai Fujii, Ryota Nakao, Saki Sugihara, Keita Fujita, Yuya Araki, Takayuki Kudoh, Ichiro Hayakawa, Haruki Mizoguchi, Akira Sakakura,* Synlett<\/em> 2020<\/strong>, 31<\/em> (20), 2013\u20132017.
DOI: 10.1055\/s-0040-1707302<\/a>
 
78. \"Kinetic Resolution of \u03b1-Nitrolactones by Catalytic Asymmetric Hydrolysis or Ester\u2013Amide Exchange Reaction\"
Ryota Nakao, Yudai Fujii, Ichiro Hayakawa, Haruki Mizoguchi, Akira Sakakura,* Synlett<\/em> 2020<\/strong>, 31<\/em> (20), 2018\u20132022.
DOI: 10.1055\/s-0040-1707303 <\/a>
 
79. \"Synthesis of functionalized cyclopropylboronic esters based on a 1,2-metallate rearrangement of cyclopropenylboronate\"
Haruki Mizoguchi,* Masaya Seriua, Akira Sakakura,* Chem. Commun.<\/em> 2020<\/strong>, 56<\/em> (99), 15545\u201315548.
DOI: 10.1039\/d0cc07134j <\/a>
 
80. \"Toward the Synthesis of Paspaline-Type Indole-Terpenes: Stereoselective Construction of Core Scaffold with Contiguous Asymmetric Quaternary Carbon Centers\"
Ichiro Hayakawa*, Naochika Matsumaru, and Akira Sakakura,* J. Org. Chem.<\/em> 2021<\/strong>, ASAP
DOI: 10.1021\/acs.joc.1c01193 <\/a>
 <\/p>\n\n\n\n

\u89e3\u8aac\uff0c\u7dcf\u8aac\u306a\u3069<\/h4>\n\n\n\n

1.\u300c\u7b2c\uff12\u7ae0\u3000\u30d5\u30eb\u30aa\u30e9\u30b9\u30b1\u30df\u30b9\u30c8\u30ea\u30fc\u306e\u57fa\u790e\u300d
\u3000John A. Gladysz\uff08\u7ffb\u8a33\uff1a\u5742\u5009\u5f70\uff0c\u77f3\u539f\u4e00\u5f70\uff09
\u3000\u30d5\u30eb\u30aa\u30e9\u30b9\u30b1\u30df\u30b9\u30c8\u30ea\u30fc<\/em>\uff0c\u76e3\u4fee\uff1a\u5927\u5bfa\u7d14\u8535\uff0c\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248, 2005<\/strong>, pp. 161\u2013169.
2.\u300c\u30d7\u30ed\u30b9\u30bf\u30b0\u30e9\u30f3\u30b8\u30f3\u306e\u9375\u4e2d\u9593\u4f53\u306e\u753b\u671f\u7684\u5408\u6210\u6cd5\u300d
\u3000\u5742\u5009\u5f70
\u3000\u5316\u5b66<\/em>\uff0c\u6ce8\u76ee\u306e\u8ad6\u6587<\/em>\uff0c\u5316\u5b66\u540c\u4eba\uff0c2006<\/strong>, 61<\/em>, 64\u201365.
3. \u300c\u74b0\u5883\u4f4e\u8ca0\u8377\u578b\u89e6\u5a92\u7684\u8131\u6c34\u53cd\u5fdc\u30d7\u30ed\u30bb\u30b9\u306e\u958b\u767a\u300d
\u3000\u5742\u5009\u5f70\uff0c\u77f3\u539f\u4e00\u5f70
\u3000\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u8a8c<\/em>, 2006<\/strong>, 64<\/em>, 651\u2013663.
\u3000\"Development of environmentally benign catalytic dehydration process\"
\u3000Akira Sakakura, Kazuaki Ishihara
\u3000Journal of Synthetic Organic Chemistry Japan<\/em> 2006<\/strong>, 64<\/em>, 651\u2013663.
4. \"Design of Highly Functional Small-Molecule Catalysts and Related Reactions Based on Acid\u2013Base Combination Chemistry\"
\u3000Kazuaki Ishihara, Akira Sakakura, Manabu Hatano
\u3000Synlett<\/em> 2007<\/strong>, 686\u2013703.
\u3000DOI: 10.1055\/s-2007-970776 <\/a>
5.\u300cSimple is best\u3067\u63b4\u3093\u3060\u601d\u308f\u306c\u5927\u767a\u898b\uff01\u2014\u7121\u5869\u57fa\u30fb\u7121\u6eb6\u5a92\u6761\u4ef6\u3067\u306eDMAP\u89e6\u5a92\u30a8\u30b9\u30c6\u30eb\u5408\u6210\u6cd5\u300d
\u3000\u5742\u5009\u5f70\uff0c\u77f3\u539f\u4e00\u5f70
\u3000\u5316\u5b66<\/em>\uff0c\u7814\u7a76\u7269\u8a9e<\/em>\uff0c2007<\/strong>, 63<\/em>, 12\u201316.
6. \"Enantioselective biomimetic polyene cyclization of polyprenoids\"
\u3000Akira Sakakura, Kazuaki Ishihara
\u3000Chimica Oggi-Chemistry Today (Suppl. Chiral Technologies)<\/em> 2007<\/strong>, 25<\/em>, 9\u201312.
7. \u300c\u9178\u30fb\u5869\u57fa\u8907\u5408\u5869\u3092\u9375\u3068\u3059\u308b\u9ad8\u6a5f\u80fd\u89e6\u5a92\u306e\u8a2d\u8a08\u304a\u3088\u3073\u9ad8\u9078\u629e\u7684\u5408\u6210\u6cd5\u306e\u958b\u62d3\u300d
\u3000\u5742\u5009\u5f70
\u3000\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u8a8c<\/em>, 2008<\/strong>, 66<\/em>, 942\u2013952.
\u3000\"Design of High-Performance Catalysts Based on Acid\u2013Base Combined Salts and Development of Highly Selective Reactions\"
\u3000Akira Sakakura
\u3000Journal of Synthetic Organic Chemistry Japan<\/em> 2008<\/strong>, 66<\/em>, 942\u2013952.
8.\u300c\u7b2c11\u7ae0\u3000\u9178\u5869\u57fa\u8907\u5408\u89e6\u5a92\u3000\u4ed8\u52a0\u74b0\u5316\u53cd\u5fdc\u3092\u4e2d\u5fc3\u3068\u3057\u3066\u300d
\u3000\u5742\u5009\u5f70\uff0c\u77f3\u539f\u4e00\u5f70
\u3000\u9032\u5316\u3092\u7d9a\u3051\u308b\u6709\u6a5f\u89e6\u5a92\u3000\u6709\u6a5f\u5408\u6210\u3092\u9769\u65b0\u3059\u308b\u7b2c\u4e09\u306e\u89e6\u5a92<\/em>\uff0c\u7de8\u96c6\uff1a\u4e38\u5ca1\u5553\u4e8c\uff0c\u5316\u5b66\u540c\u4eba\uff0c2009<\/strong>, pp. 128\u2013135.
9. \"Organoammonium Salt-Catalyzed Enantioselective Cycloaddition Reactions with \u03b1-(Acyloxy)- or \u03b1-Diacylaminoacroleins\"
\u3000Akira Sakakura, Kazuaki Ishihara
\u3000Bull. Chem. Soc. Jpn<\/em> 2010<\/strong>, 83<\/em>, 313\u2013322.
\u3000DOI: 10.1246\/bcsj.20090345 <\/a>
 10.\u300c\u5f31\u3044\u4e8c\u6b21\u7684\u76f8\u4e92\u4f5c\u7528\u3092\u9375\u3068\u3059\u308b\u4e0d\u6589\u89e6\u5a92\u306e\u7cbe\u5bc6\u8a2d\u8a08\u2014\u30eb\u30a4\u30b9\u5869\u57fa\u306b\u3088\u308b\u30eb\u30a4\u30b9\u9178\u89e6\u5a92\u306e\u6d3b\u6027\u5316\u3068\u67d4\u8edf\u306a\u4e0d\u6589\u53cd\u5fdc\u5834\u306e\u69cb\u7bc9\u300d
\u3000\u5742\u5009\u5f70
\u3000\u5316\u5b66\u3068\u5de5\u696d<\/em>\uff0c\u652f\u90e8\u767a\u8a71\u984c\u6b04<\/em>\uff0c2010<\/strong>, (3), 238\u2013239.
11. \"Asymmetric Cu(II) catalyses for cycloaddition reactions based on \u03c0\u2013cation or n\u2013cation interaction\"
\u3000Akira Sakakura, Kazuaki Ishihara
\u3000Chem. Soc. Rev.<\/em> 2011<\/strong>, 40<\/em>, 163\u2013172.
\u3000DOI: 10.1039\/B924478F <\/a>
12. \u201c3.2 [4+2]-Cycloaddition Reactions\u201d
\u3000Kazuaki Ishihara, Akira Sakakura
\u3000In Science of Synthesis, Stereoselective Synthesis 3: Stereoselective Pericyclic Reactions, Cross Coupling, and C\u2013H and C\u2013X Activation<\/em>;
\u3000Evans, P. A., Ed., Georg Thieme Verlag: Stuttgart, 2011<\/strong>, pp. 67\u2013123.
13. \u201c7.10 C\u2013C bond formation | Diels\u2013Alder reaction\u201d
\u3000Kazuaki Ishihara, Akira Sakakura
\u3000In Comprehensive Chirality: Synthetic Methods V \u2013 Organocatalysis<\/em>; Hisashi Yamamoto and Eric Carreira, Eds., Elsevier: Oxford, 2012<\/strong>, pp. 264\u2013292.
\u3000DOI: 10.1016\/B978-0-08-095167-6.00610-8 <\/a>
14. \"5.9 Intermolecular Diels\u2013Alder Reactions\"
\u3000Kazuaki Ishihaira, Akira Sakakura
\u3000In Comprehensive Organic Synthesis<\/em>, 2nd Edition, Vol. 5, Gary A. Molander and Paul Knochel (eds.), Oxford: Elsevier; 2014<\/strong>, pp. 351-408.
15. \"5.10 Hetero-Diels\u2013Alder Reactions\"
\u3000Kazuaki Ishihaira, Akira Sakakura
\u3000In Comprehensive Organic Synthesis<\/em>, 2nd Edition, Vol. 5, Gary A. Molander and Paul Knochel (eds.), Oxford: Elsevier; 2014<\/strong>, pp. 409-465.
16.  \u201cCopper(II) Triflimide\u201d
\u3000Akira Sakakura, Kazuaki Ishihara
\u3000In e-EROS (Encyclopedia of Reagents for Organic Synthesis)<\/em>; Wiley, 2017<\/strong>, Chapter April 2017, pp. 1\u20134.
\u3000DOI: 10.1002\/047084289X.rn01746 <\/a>
\u3000First published : 10 April 2017
17. \u300c\u30c1\u30bf\u30f3\u3092\u7528\u3044\u308b\u30af\u30ed\u30b9\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\uff0d\u30b9\u30c6\u30ed\u30a4\u30c9\u3084\u30c6\u30eb\u30da\u30ce\u30a4\u30c9\u5408\u6210\u3078\u306e\u65b0\u305f\u306a\u30a2\u30d7\u30ed\u30fc\u30c1\u300d
\u3000\u6e9d\u53e3\u7384\u6a39\uff0c\u5742\u5009\u5f70
\u3000\u5316\u5b66<\/em>\uff0c\u6700\u65b0\u306e\u30c8\u30d4\u30c3\u30af\u30b9<\/em>\uff0c\u5316\u5b66\u540c\u4eba\uff0c2018<\/strong>, 73<\/em>, 68\u201369.
18. \"Strain-Release Difunctionalization of C\u2013C \u03c3- and \u03c0-bonds of an Organoboron Ate-Complex through 1,2-Metallate Rearrangement\"
  Haruki Mizoguchi,* Akira Sakakura,* Chem. Lett.<\/em> 2021<\/strong>, 50<\/em> (4), 792\u2013799.
  DOI: 10.1246\/cl.200926 <\/a><\/p>\n","protected":false},"excerpt":{"rendered":"

\u5742\u5009\u3000\u5f70\u3000\uff08SAKAKURA Akira\uff09 \u5ca1\u5c71\u5927\u5b66\u5b66\u8853\u7814\u7a76\u9662\u74b0\u5883\u751f\u547d\u81ea\u7136\u79d1\u5b66\u5b66\u57df\u5fdc\u7528\u5316\u5b66\u5c02\u653b\u3000\u5fdc\u7528\u5316\u5b66\u8b1b\u5ea7\u00a0\u6559\u6388\u00a0 \u3012700-8530\u00a0\u5ca1\u5c71\u5e02\u5317\u533a\u6d25\u5cf6\u4e2d3-1-1\u3000\u5de5\u5b66\u90e86\u53f7\u9928361\u5ba4\u00a0TEL&FAX: \u00a008 […]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"vkexunit_cta_each_option":"","footnotes":""},"class_list":["post-38","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"http:\/\/achem.okayama-u.ac.jp\/bioorgchem\/wp-json\/wp\/v2\/pages\/38","targetHints":{"allow":["GET"]}}],"collection":[{"href":"http:\/\/achem.okayama-u.ac.jp\/bioorgchem\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"http:\/\/achem.okayama-u.ac.jp\/bioorgchem\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"http:\/\/achem.okayama-u.ac.jp\/bioorgchem\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/achem.okayama-u.ac.jp\/bioorgchem\/wp-json\/wp\/v2\/comments?post=38"}],"version-history":[{"count":4,"href":"http:\/\/achem.okayama-u.ac.jp\/bioorgchem\/wp-json\/wp\/v2\/pages\/38\/revisions"}],"predecessor-version":[{"id":422,"href":"http:\/\/achem.okayama-u.ac.jp\/bioorgchem\/wp-json\/wp\/v2\/pages\/38\/revisions\/422"}],"wp:attachment":[{"href":"http:\/\/achem.okayama-u.ac.jp\/bioorgchem\/wp-json\/wp\/v2\/media?parent=38"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}