Oyo Mitsunobu
 | This article has been nominated for merging into Mitsunobu reaction. You are welcome to participate in the merging discussion, which will decide whether to merge it into Mitsunobu reaction. This discussion may also result in the article being deleted, redirected, or draftified. |
Ōyō Mitsunobu (光延 旺洋, Mitsunobu Ōyō; 1934–2003) was a Japanese chemist specializing in organic synthesis. In 1967, he introduced the Mitsunobu reaction,[1][2] which is named after him.
His father was Tōyō Mitsunobu, an admiral (posthumously) of the Japanese navy.[3] Mitsunobu earned his bachelor's degree at Gakushuin University in Tokyo and subsequently studied at the Tokyo Institute of Technology starting in 1959, where he obtained his doctorate in 1966 under the supervision of Teruaki Mukaiyama.[4] From 1986-2002 he was a Professor in the Faculty of Science and Engineering, Aoymam Gakuin Univeristy.[5]
His work focused on the chemistry of nucleosides and nucleotides, as well as stereoselective reactions. He is best know for the Mitsunobu reaction which involves the substitution of (primary or secondary) alcohols with nucleophiles (the original reaction was an esterification) and has found widespread application, particularly in the synthesis of natural products and in biochemistry. It proceeds under relatively mild conditions and is stereospecific. It is an oxidation-reduction condensation reaction in which triphenylphosphine is oxidized and diethyl azodicarboxylate (DEAD) is reduced to its corresponding hydrazine derivative (reagents serving a similar function to triphenylphosphine and DEAD in the original version of the reaction are known as Mitsunobu reagents). Mitsunobu introduced the reaction in 1967 and developed several variants shortly thereafter. Between 1996 and 2008, 1,615 papers with "Mitsunobu reaction" in the title were published according to SciFinder, including 186 patents.[6]
In 1984 he received the Synthetic Organic Chemistry Award, Japan. The text of the award states that it is for the "Discovery and development of stereospecific reactions through activation of alcoholic hydroxyl groups (アルコール性水酸基の活性化による立体特異的反応の発見とその展開)".[7]
References
[edit]- ↑ Mitsunobu, Oyo; Yamada, Masaaki (1967-10-01). "Preparation of Esters of Carboxylic and Phosphoric Acid via Quaternary Phosphonium Salts". Bulletin of the Chemical Society of Japan. 40 (10): 2380–2382. doi:10.1246/bcsj.40.2380. ISSN 0009-2673.
- ↑ Mitsunobu, Oyo (1981). "The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products". Synthesis. 1981 (01): 1–28. doi:10.1055/s-1981-29317. ISSN 0039-7881.
- ↑ "光延旺洋とは - わかりやすく解説 Weblio辞書". www.weblio.jp. Retrieved 2026-08-11.
- ↑ Murakami, Masahiro (2021). "Achievements of the Late Professor Teruaki Mukaiyama". The Chemical Record. 21 (1): 2–16. doi:10.1002/tcr.202000105. ISSN 1528-0691.
- ↑ "光延 旺洋". KAKEN. Retrieved 2026-08-11.
- ↑ K. C. Kumara Swamy, N. N. Bhuvan Kumar, E. Balaraman, V. P. Pavan Kumar, Mitsunobu and related reactions, Chemical Reviews, Vol. 109, 2009, pp. 2551–2651
- ↑ "有機合成化学協会賞 | 公益社団法人 有機合成化学協会 | SSOCJ – The Society of Synthetic Organic Chemistry, Japan". 有機合成化学協会賞 | 公益社団法人 有機合成化学協会 | SSOCJ – The Society of Synthetic Organic Chemistry, Japan (in Japanese). Retrieved 2026-08-11.
,