{"id":34,"date":"2021-11-24T11:09:51","date_gmt":"2021-11-24T02:09:51","guid":{"rendered":"http:\/\/achem.okayama-u.ac.jp\/bioorgchem\/WordPress\/?page_id=34"},"modified":"2025-08-29T10:00:28","modified_gmt":"2025-08-29T01:00:28","slug":"member%ef%bc%88hm%ef%bc%89","status":"publish","type":"page","link":"http:\/\/achem.okayama-u.ac.jp\/bioorgchem\/member%ef%bc%88hm%ef%bc%89","title":{"rendered":"Member\uff08HM\uff09"},"content":{"rendered":"\n

\u6e9d\u53e3\u3000\u7384\u6a39\u3000\uff08MIZOGUCHI Haruki\uff09<\/strong><\/p>\n\n\n\n

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

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TEL:  086-251-8211 
E-mail: h_mizoguchi\uff20okayama-u.ac.jp 
ORCID: 0000-0002-2148-9699 <\/a><\/p>\n\n\n\n

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2010\u5e74\u3000\u5317\u6d77\u9053\u5927\u5b66\u5927\u5b66\u9662\u7406\u5b66\u9662\u5316\u5b66\u5c02\u653b \u4fee\u58eb\u8ab2\u7a0b\u4fee\u4e86\uff08\u53ca\u5ddd\u82f1\u79cb\u6559\u6388\u30fb\u5927\u6817\u535a\u6bc5\u51c6\u6559\u6388\uff09
2013\u5e74\u3000\u5317\u6d77\u9053\u5927\u5b66\u5927\u5b66\u9662\u7dcf\u5408\u5316\u5b66\u9662\u7dcf\u5408\u5316\u5b66\u5c02\u653b \u535a\u58eb\u5f8c\u671f\u8ab2\u7a0b\u4fee\u4e86\uff08\u53ca\u5ddd\u82f1\u79cb\u6559\u6388\u30fb\u5927\u6817\u535a\u6bc5\u51c6\u6559\u6388\uff09
2013\u5e74\u3000\u535a\u58eb\uff08\u7406\u5b66\uff09\u53d6\u5f97\uff08\u5317\u6d77\u9053\u5927\u5b66\uff09<\/p>\n\n\n\n

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2010\u5e74\u3000\u65e5\u672c\u5b66\u8853\u632f\u8208\u4f1a\u7279\u5225\u7814\u7a76\u54e1\uff08\uff24\uff23\uff11\uff09\uff08\u5317\u6d77\u9053\u5927\u5b66\uff09
2013\u5e74\u3000\u5317\u6d77\u9053\u5927\u5b66\u5927\u5b66\u9662\u7406\u5b66\u7814\u7a76\u9662\u3000\u535a\u58eb\u7814\u7a76\u54e1\uff08\u7814\u7a76\u5ba4\u4e3b\u5bb0\uff1a\u5927\u6817\u535a\u6bc5\u51c6\u6559\u6388\uff09
2013\u5e74\u3000\u7c73\u56fd\u30c0\u30fc\u30c8\u30de\u30b9\u5927\u5b66\u5316\u5b66\u79d1\u3000\u535a\u58eb\u7814\u7a76\u54e1\uff08\u7814\u7a76\u5ba4\u4e3b\u5bb0\uff1aGlenn C. Micalizio\u6559\u6388\uff09
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2013\u5e74\u301c2014\u5e74\u3000\u4e0a\u539f\u8a18\u5ff5\u751f\u547d\u79d1\u5b66\u8ca1\u56e3\u3000\u6d77\u5916\u7559\u5b66\u52a9\u6210\u3000\u30dd\u30b9\u30c8\u30c9\u30af\u30c8\u30e9\u30eb\u30d5\u30a7\u30ed\u30fc\u30b7\u30c3\u30d7
2015\u5e74\u301c2017\u5e74\u3000\u65e5\u672c\u5b66\u8853\u632f\u8208\u4f1a\u6d77\u5916\u7279\u5225\u7814\u7a76\u54e1
2017\u5e74\u3000\u5ca1\u5c71\u5927\u5b66\u5927\u5b66\u9662\u81ea\u7136\u79d1\u5b66\u7814\u7a76\u79d1\uff08\u5de5\u5b66\u7cfb\uff09\u52a9\u6559\uff08\u7814\u7a76\u5ba4\u4e3b\u5bb0\uff1a\u5742\u5009\u5f70\u6559\u6388\uff09<\/p>\n\n\n\n

2021\u5e74\u3000\u5ca1\u5c71\u5927\u5b66\u5b66\u8853\u7814\u7a76\u9662\u81ea\u7136\u79d1\u5b66\u5b66\u57df\u3000\u51c6\u6559\u6388\uff08\u7814\u7a76\u5ba4\u4e3b\u5bb0\uff1a\u5742\u5009\u5f70\u6559\u6388\uff09
2123\u5e74\u3000\u6539\u7d44\u306b\u3088\u308a\u5ca1\u5c71\u5927\u5b66\u5b66\u8853\u7814\u7a76\u9662\u74b0\u5883\u751f\u547d\u81ea\u7136\u79d1\u5b66\u5b66\u57df\u306b\u6240\u5c5e\u5909\u66f4<\/p>\n\n\n\n

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1. \u8ca1\u56e3\u6cd5\u4eba\u5317\u6d77\u9053\u5927\u5b66\u30af\u30e9\u30fc\u30af\u8a18\u5ff5\u8ca1\u56e3\u3000\u30af\u30e9\u30fc\u30af\u8cde\uff082008\u5e74\uff09
2. \u7b2c22\u56de\u4e07\u6709\u672d\u5e4c\u30b7\u30f3\u30dd\u30b8\u30a6\u30e0\u3000\u30dd\u30b9\u30bf\u30fc\u7279\u5225\u8cde\uff082010\u5e74\uff09
3. \u7b2c\u4e00\u56de\u5927\u6d25\u4f1a\u8b70\u30a2\u30ef\u30fc\u30c9\u30d5\u30a7\u30ed\u30fc\uff082010\u5e74\uff09
4. \u7b2c102\u56de\u6709\u6a5f\u5408\u6210\u30b7\u30f3\u30dd\u30b8\u30a6\u30e0\u3000\u512a\u79c0\u30dd\u30b9\u30bf\u30fc\u8cde\uff082012\u5e74\uff09
5. 2014 Reaxys PhD Prize Finalist\uff082014\u5e74\uff09
6. \u5e73\u621030\u5e74\u5ea6\u5929\u7136\u7269\u5316\u5b66\u8ac7\u8a71\u4f1a\u5968\u52b1\u8cde\uff082018\u5e74\uff09
\u3000\u300c\u4f4e\u539f\u5b50\u4fa1\u30c1\u30bf\u30f3\u3092\u7528\u3044\u308b\u70ad\u7d20\u9aa8\u683c\u306e\u7acb\u4f53\u9078\u629e\u7684\u5408\u6210\u6cd5\u306e\u958b\u767a\u300d
7. \u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u3000\u4e2d\u5916\u88fd\u85ac\u7814\u7a76\u4f01\u753b\u8cde\uff082018\u5e74\uff09
\u3000\u300c\u30db\u30a6\u7d20\u30a2\u30fc\u30c8\u932f\u4f53\u306e1,2-\u30e1\u30bf\u30ec\u30fc\u30c8\u8ee2\u4f4d\u3092\u7cbe\u5bc6\u5236\u5fa1\u3059\u308b\u591a\u5b98\u80fd\u6027\u5206\u5b50\u9aa8\u683c\u306e\u69cb\u7bc9\u300d
8. \u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u3000\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5968\u52b1\u8cde\uff082024\u5e74\uff09
\u3000\u300c\u30db\u30a6\u7d20\u30a2\u30fc\u30c8\u932f\u4f53\u306e\u7279\u6027\u3092\u6d3b\u304b\u3057\u305f\u5206\u5b50\u69cb\u7bc9\u6cd5\u306e\u958b\u767a\u300d<\/p>\n\n\n\n

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

1. \"Divergent and Expeditious Access to Fused Skeletons Inspired by Indole Alkaloids and Transtaganolides\"
Haruki Mizoguchi, Hiroki Oguri, Kiyoshi Tsuge, Hideaki Oikawa, Org. Lett.<\/em> 2009<\/strong>, 11<\/em> (14), 3016\u20133019.
DOI: 10.1021\/ol901020a <\/a>
 
2. \"Hg(OTf)2-catalyzed direct vinylation of tryptamines and versatile applications for tandem reactions\"
Haruki Mizoguchi, Hideaki Oikawa, Hiroki Oguri, Org. Biomol. Chem.<\/em> 2012<\/strong>, 10<\/em> (21), 4236\u20134242.
DOI: 10.1039\/C2OB25236H <\/a>
 
3. \"Parallel and four-step synthesis of natural-product-inspired scaffolds through modular assembly and divergent cyclization\"
Hiroki Oguri, Haruki Mizoguchi, Hideaki Oikawa, Aki Ishiyama, Masato Iwatsuki, Kazuhiko Otoguro, Satoshi \u014cmura, Beilsterin J. Org. Chem.<\/em> 2012<\/strong>, 8<\/em>, 930\u2013940.
DOI: 10.3762\/bjoc.8.105 <\/a>
 
4. \"Biogenetically inspired synthesis and skeletal diversification of indole alkaloids\"
Haruki Mizoguchi, Hideaki Oikawa, Hiroki Oguri, Nat. Chem.<\/em> 2014<\/strong>, 6<\/em> (1), 57\u201364.
DOI: 10.1038\/nchem.1798 <\/a>
 
5. \"Synthesis of Angularly Substituted Trans-Fused Hydroindanes by Convergent Coupling of Acyclic Precursors\"
Valer Jeso, Claudio Aquino, Xiayun Cheng, Haruki Mizoguchi, Mika Nakashige, Glenn C. Micalizio, J. Am. Chem. Soc.<\/em> 2014<\/strong>, 136<\/em> (23), 8209\u20138212.
DOI: 10.1021\/ja504374j <\/a>
 
6. \"LiOOt-Bu as a terminal oxidant in a titanium alkoxide-mediated [2+2+2] reaction cascade\"
Wan Shin Kim, Claudio Aquino, Haruki Mizoguchi, Glenn C. Micalizio, Tetrahedron Lett.<\/em> 2015<\/strong>, 56<\/em> (23), 3557\u20133559.
DOI: 10.1016\/j.tetlet.2015.01.029 <\/a>
 
7. \"Synthesis of multiply substituted 1,6-dihydropyridines through Cu(I)-catalyzed 6-endo cyclization\"
Haruki Mizoguchi, Ryo Watanabe, Shintaro Minami, Hideaki Oikawa, Hiroki Oguri, Org. Biomol. Chem.<\/em> 2015<\/strong>, 13<\/em> (21), 5955\u20135963.
DOI: 10.1039\/C5OB00356C <\/a>
 
8. \"Synthesis of Highly Functionalized Decalins via Metallacycle-Mediated Cross-Coupling\"
Haruki Mizoguchi, Glenn C. Micalizio, J. Am. Chem. Soc.<\/em> 2015<\/strong>, 137<\/em> (20), 6624\u20136628.
DOI: 10.1021\/jacs.5b02107 <\/a>
 
9. \"Acceleration of metallacycle-mediated alkyne-alkyne cross-coupling with TMSCl\"
James S. Cassidy, Haruki Mizoguchi, Glenn C. Micalizio, Tetrahedron Lett.<\/em> 2016<\/strong>, 57<\/em> (34), 3848\u20133850.
DOI: 10.1016\/j.tetlet.2016.07.045 <\/a>
 
10. \"Synthesis of Angularly Substituted trans-Fused Decalins through a Metallacycle-Mediated Annulative Cross-Coupling Cascade\"
Haruki Mizoguchi, Glenn. C. Micalizio, Angew. Chem. Int. Ed.<\/em> 2016<\/strong>, 55<\/em> (42), 13099\u201313103.
DOI: 10.1002\/anie.201606962 <\/a>
 
11. \"Stereo-controlled synthesis of functionalized tetrahydropyridines based on the cyanomethylation of 1,6-dihydropyridines and generation of anti-hepatitis C virus agents\"
Ryo Watanabe, Haruki Mizoguchi, Hideaki Oikawa, Hirofumi Ohashi, Koichi Watashi, Hiroki Oguri, Bioorg. Med. Chem.<\/em> 2017<\/strong>, 25<\/em> (11), 2851\u20132855.
DOI: 10.1016\/j.bmc.2017.03.011 <\/a>
 
12. \"Design and De Novo Synthesis of 6-Aza-artemisinins\"
Karunakar Reddy Bonepally, Takahisa Hiruma, Haruki Mizoguchi, Kyohei Ochiai, Shun Suzuki, Hideaki Oikara, Aki Ishiyama, Rei Hokari, Masato Iwatsuki, Kazuhiko Otoguro, Satoshi \u014cmura, Hiroki Oguri, Org Lett.<\/em> 2018<\/strong>, 20<\/em> (15), 4667-4671.
DOI: 10.1021\/acs.orglett.8b01987 <\/a>
 
13. \"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>
 
14. \"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>
 
15. \"Zn(OTf)2-mediated annulations of N-propargylated tetrahydrocarbolines: divergent synthesis of four distinct alkaloidal scaffolds\"
Sadaiwa Yorimoto, Akira Tsubouchi, Haruki Mizoguchi, Hideaki Oikawa, Yoshiaki Tsunekawa, Tomoya Ichino, Satoshi Maeda,* Hiroki Oguri,* Chem. Sci.<\/em> 2019<\/strong>, 10<\/em> (22), 5686\u20135698.
DOI: 10.1039\/C9SC01507H <\/a>
 
16. \"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>
 
17. \"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>
 
18. \"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>
 
19. \"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><\/p>\n\n\n\n

20. \"Enantioselective construction of \u03b2-hydroxy-\u03b1,\u03b1-disubstituted \u03b1-amino acid derivatives via direct aldol reaction of \u03b1-imino esters\"
Yuya Araki, Masato Hanada, Yoshiko Iguchi, Haruki Mizoguchi, Akira Sakakura*
Tetrahedron<\/em> 2022<\/strong>, 110<\/em>, 132695.  DOI: 10.1016\/j.tet.2022.132695<\/a><\/em><\/p>\n\n\n\n

21. \"Annulative coupling of vinylboronic esters: aryne-triggered 1,2-metallate rearrangement\"
Haruki Mizoguchi*, Hidetoshi Kamada, Kazuki Morimoto, Ryuji Yoshida, Akira Sakakura*
Chem. Sci.<\/em> 2022<\/strong>, 13<\/em>, 9580\u20139585.
DOI: \/10.1039\/D2SC02623F<\/p>\n\n\n\n

22. \"Visible-Light-Photoexcited Palladium-Catalyzed Silylmethylation of Benzyl Alcohol Derivatives\"
Haruki Mizoguchi*,Ryuji Yoshida, Haruka Ikeda, Akira Sakakura*
Synlett<\/em> 2023<\/strong>, eFirst (Special Issue Dedicated to Prof. Hisashi Yamamoto)<\/em>
DOI: 10.1055\/s-0042-1752736<\/p>\n\n\n\n

23. \"Rapid construction of a diterpene-inspired tetracyclic skeleton bearing bicyclo[3.2.1]octane rings based on desymmetrization of 1,3-diketones\"
Hidetoshi Kamada, Haruki Mizoguchi*, Akira Sakakura*
Tetrahedron<\/em>\u00a0Lett. 2025<\/strong>,\u00a0157<\/em>, 155470.\u00a0 DOI:\u00a0<\/a>10.1016\/j.tetlet.2025.155470<\/a><\/em><\/p>\n\n\n\n

24. \"Synthesis of an Angular Triquinane Structure Based on a Stereoselective Decarboxylative Giese Reaction at an Angular Position in a Diquinane Skeleton\"
Naochika Matsumaru, Takumu Nishitani, Haruki Mizoguchi*, Akira Sakakura*
Tetrahedron<\/em> 2025<\/strong>,\u00a0178<\/em>, 134612.\u00a0 DOI:\u00a010.1016\/j.tet.2025.134612<\/a><\/em><\/p>\n\n\n\n

24. \"Development of a Vinylated Cyclic Allene: A Fleeting Strained Diene for the Diels\u2013Alder Reaction\"
Haruki\u00a0Mizoguchi*,\u00a0Takumi Obata, Taiki Hirai, Manaka Komatsu, Akira\u00a0Sakakura*
Angew. Chem. Int. Ed.\u00a0<\/em>2025<\/strong>,\u00a0<\/em>64, e202510319<\/em>\u00a0 DOI:\u00a010.1002\/anie.202510319<\/a><\/a><\/em>

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

1. \u300c\u751f\u5408\u6210\u7d4c\u8def\u3092\u6a21\u5023\u3057\u305f\u9aa8\u683c\u591a\u69d8\u5316\u5408\u6210\u2014\u30cb\u30c1\u30cb\u30c1\u30bd\u30a6\u306b\u5b66\u3076\u30a2\u30eb\u30ab\u30ed\u30a4\u30c9\u9aa8\u683c\u306e\u4f5c\u308a\u5206\u3051\u300d
\u3000\u5927\u6817\u535a\u6bc5\uff0c\u6e9d\u53e3\u7384\u6a39
\u3000\u5316\u5b66<\/em>, 2014<\/strong>, 69<\/em>, 12\u201317.
2. \u300c\u30a4\u30f3\u30c9\u30fc\u30eb\u30a2\u30eb\u30ab\u30ed\u30a4\u30c9\u306e\u9aa8\u683c\u591a\u69d8\u5316\u5408\u6210\u2014\u751f\u5408\u6210\u306b\u5b66\u3076\u5206\u5c90\u578b\u5408\u6210\u6226\u7565\u2014\u300d
\u3000\u6e9d\u53e3\u7384\u6a39\uff0c\u5927\u6817\u535a\u6bc5
\u3000\u5316\u5b66\u3068\u751f\u7269<\/em>, 2015<\/strong>, 53<\/em>, 345\u2013346.
3. \u300c\u751f\u5408\u6210\u7d4c\u8def\u3092\u6a21\u5023\u3057\u305f\u30a4\u30f3\u30c9\u30fc\u30eb\u30a2\u30eb\u30ab\u30ed\u30a4\u30c9\u7fa4\u306e\u9aa8\u683c\u591a\u69d8\u5316\u5408\u6210\u300d
\u3000\u6e9d\u53e3\u7384\u6a39\uff0c\u5927\u6817\u535a\u6bc5
\u3000\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u8a8c<\/em>\uff0c2016<\/strong>, 74<\/em>, 854\u2013865.
4. \u201cThe Development of Alkoxide-Directed Metallacycle-Mediated Annulative Cross-Coupling Chemistry\u201d
\u3000Glenn C. Micalizio, Haruki Mizoguchi
\u3000Invited review in an issue dedicated to Professor Stuart L. Schreiber and K. C. Nicolaou for their receipt of Wolf Prize \u2013 <\/em>
\u3000Isr. J. Chem.<\/em> 2017<\/strong>, 57<\/em>, 228\u2013238.
\u3000DOI: 10.1002\/ijch.201600098
5. \u300c\u9ad8\u9178\u5316\u578b\u30ab\u30eb\u30c7\u30ce\u30e9\u30a4\u30c9\u306e\u52b9\u7387\u7684\u5408\u6210\uff08Review de Debut\uff09\u300d
\u3000\u6e9d\u53e3\u7384\u6a39
\u3000\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u8a8c<\/em>, 2017<\/strong>, 75<\/em>, 253\u2013254.
6.\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> (8), 68\u201369. 
7. \u300c\u751f\u7406\u6d3b\u6027\u767a\u73fe\u306e\u305f\u3081\u306e\u6d3b\u6027\u5316\u578b\u69cb\u9020\u306e\u63d0\u6848\uff1aMyrocin G\u306e\u5408\u6210\u300d
\u3000\u6e9d\u53e3\u7384\u6a39
\u3000\u30d5\u30a1\u30eb\u30de\u30b7\u30a2<\/em>\uff0c\u30c8\u30d4\u30c3\u30af\u30b9<\/em>\uff0c2019<\/strong>, 55<\/em> (10), 976.
8. \"Strain-Release Difunctionalization of C\u2013C \u03c3- and \u03c0-bonds of an Organoboron Ate-Complex through 1,2-Metallate Rearrangement\"
\u3000Haruki Mizoguchi,* Akira Sakakura,* Chem. Lett.<\/em> 2021<\/strong>, 50<\/em> (4), 792\u2013799.
\u3000DOI: 10.1246\/cl.200926 <\/a>
9. \u300c\u30d3\u30b7\u30af\u30ed[3.2.1]\u30aa\u30af\u30bf\u30f3\u7e2e\u74b0\u578b\u5929\u7136\u7269\u30b0\u30e9\u30e4\u30ca\u30f3\u30b8\u30c6\u30eb\u30da\u30ce\u30a4\u30c9\u306e\u5168\u5408\u6210\u300d
\u3000\u6e9d\u53e3\u7384\u6a39
\u3000\u5316\u5b66\u3068\u5de5\u696d\uff0c2023, 76<\/strong>(4)<\/p>\n\n\n\n

\u62db\u5f85\u8b1b\u6f14\u306a\u3069<\/h4>\n\n\n\n

1.\u300c\u30db\u30a6\u7d20\u30a2\u30fc\u30c8\u932f\u4f53\u306e1,2-\u30e1\u30bf\u30ec\u30fc\u30c8\u8ee2\u4f4d\u3092\u6d3b\u7528\u3059\u308b\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u53cd\u5fdc\u306e\u958b\u767a\u300d
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\uff12.\u300c\u30db\u30a6\u7d20\u30a2\u30fc\u30c8\u932f\u4f53\u306e\u30e1\u30bf\u30ec\u30fc\u30c8\u8ee2\u4f4d\u3092\u5229\u7528\u3059\u308b\u5206\u5b50\u69cb\u7bc9\u6cd5\u306e\u958b\u767a\u300d
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2022\u5e74\u65e5\u672c\u5316\u5b66\u4f1a\u4e2d\u56fd\u56db\u56fd\u652f\u90e8\u5927\u4f1a \u5e83\u5cf6\u5927\u4f1a\uff0c\u62db\u5f85\u516c\u6f14\uff0c\u5e83\u5cf6\uff0c2022\u5e7411\u670813\u65e5<\/p>\n\n\n\n

3.\u300c\u30db\u30a6\u7d20\u30a2\u30fc\u30c8\u932f\u4f53\u306e\u30e1\u30bf\u30ec\u30fc\u30c8\u8ee2\u4f4d\u3092\u4e2d\u5fc3\u3068\u3059\u308b\u5206\u5b50\u69cb\u7bc9\u300d
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4.\u300c\u30db\u30a6\u7d20\u304c\u4e3b\u5f79\u3068\u306a\u308b\u30a2\u30fc\u30c8\u306a\u53cd\u5fdc\u306e\u958b\u767a\u3092\u76ee\u6307\u3057\u3066\u300d
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\u6e9d\u53e3\u3000\u7384\u6a39\u3000\uff08MIZOGUCHI Haruki\uff09 \u5ca1\u5c71\u5927\u5b66\u5b66\u8853\u7814\u7a76\u9662\u74b0\u5883\u751f\u547d\u81ea\u7136\u79d1\u5b66\u5b66\u57df\uff08\u5de5\u5b66\u7cfb\uff09 \u5fdc\u7528\u5316\u5b66\u5c02\u653b\u51c6\u6559\u6388  \u3012700-8530 \u5ca1\u5c71\u5e02\u5317\u533a\u6d25\u5cf6\u4e2d3-1-1\u3000\u5de5\u5b66\u90e86\u53f7\u9928352\u5ba4 […]<\/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-34","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"http:\/\/achem.okayama-u.ac.jp\/bioorgchem\/wp-json\/wp\/v2\/pages\/34","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=34"}],"version-history":[{"count":11,"href":"http:\/\/achem.okayama-u.ac.jp\/bioorgchem\/wp-json\/wp\/v2\/pages\/34\/revisions"}],"predecessor-version":[{"id":493,"href":"http:\/\/achem.okayama-u.ac.jp\/bioorgchem\/wp-json\/wp\/v2\/pages\/34\/revisions\/493"}],"wp:attachment":[{"href":"http:\/\/achem.okayama-u.ac.jp\/bioorgchem\/wp-json\/wp\/v2\/media?parent=34"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}