Tohru Fukuyama

The native form of this personal name is Fukuyama Tōru. This article uses Western name order when mentioning individuals.

Tohru Fukuyama
Tohru Fukuyama
Born	(1948-08-09) August 9, 1948 Anjō, Aichi, Japan
Alma mater	Nagoya University Harvard University
Known for	Fukuyama coupling
Scientific career
Institutions	Harvard University Rice University University of Tokyo
Thesis	The total synthesis of gliotoxin (1977)
Doctoral advisor	Yoshito Kishi

Tohru Fukuyama (福山 透, Fukuyama Tōru, born 9 August 1948) is a Japanese organic chemist and Professor of Chemistry at University of Tokyo in Japan. He discovered the Fukuyama coupling in 1998.

Biography

Fukuyama studied chemistry at Nagoya University with degrees Bachelor's (1971) and Master's (1973) degrees. As a graduate student, he then worked at Harvard University, where he received his doctorate in 1977 as an academic student of Yoshito Kishi. Until 1978, he continued his research as a postdoc in the Department of Chemistry of Harvard University and then moved to Rice University as an assistant professor, where in 1988 he obtained the rank of a chair holder. In 1995, he accepted a professorship in Pharmaceutical Sciences from the University of Tokyo, Japan. Since 2013, Fukuyama has been working as a professor at the Nagoya University - more precisely: Designated Professor of Pharmaceutical Sciences.

The 2015 Nobel Prize in Physiology or Medicine winner Satoshi Ōmura is his old friend.

Achievements

• Fukuyama reduction
• Fukuyama indole synthesis
• Fukuyama coupling

Selected publications

• Practical Total Synthesis of (±)-Mitomycin C, T. Fukuyama and L.-H. Yang, J. Am. Chem. Soc., 111, 8303–8304 (1989).
• Facile Reduction of Ethyl Thiol Esters to Aldehydes: Application to a Total Synthesis of ( )-Neothramycin A Methyl Ether, T. Fukuyama, S.-C. Lin, and L.-P. Li, J. Am. Chem. Soc., 112, 7050–7051 (1990).
• Total Synthesis of ( )-Leinamycin, Y. Kanda and T. Fukuyama, J. Am. Chem. Soc., 115, 8451–8452 (1993).
• 2- and 4-Nitrobenzenesulfonamides: Exceptionally Versatile Means for Preparation of Secondary Amines and Protection of Amines, T. Fukuyama, C.-K. Jow, and M. Cheung, Tetrahedron Lett., 36, 6373–6374 (1995).
• “Radical Cyclization of 2-Alkenylthioanilides: A Novel Synthesis of 2,3-Disubstituted Indoles,” H. Tokuyama, T. Yamashita, M. T. Reding, Y. Kaburagi, and T. Fukuyama, J. Am. Chem. Soc., 121, 3791–3792 (1999).
• Stereocontrolled Total Synthesis of ( )-Vinblastine, S. Yokoshima, T. Ueda, S. Kobayashi, A. Sato, T. Kuboyama, H. Tokuyama, and T. Fukuyama, J. Am. Chem. Soc., 124, 2137–2139 (2002).
• Total Synthesis of ( )-Yatakemycin, K. Okano, H. Tokuyama, and T. Fukuyama, J. Am. Chem. Soc., 128, 7136–7137 (2006).
• A Practical Synthesis of (–)-Oseltamivir, N. Satoh, T. Akiba, S. Yokoshima, and T. Fukuyama, Angew. Chem. Int. Ed., 46, 5734–5736 (2007).
• A Practical Synthesis of (–)-Kainic Acid, S. Takita, S. Yokoshima, and T. Fukuyama, Org. Lett., 13, 2068–2070 (2011).
• Total Synthesis of Ecteinascidin 743, F. Kawagishi, T. Toma, T. Inui, S. Yokoshima, and T. Fukuyama, J. Am. Chem. Soc., 135, 13684–13687 (2013).

References

• "Advisory Board: Tohru Fukuyama". Royal Society Publishing.
• Homepage of Tohru Fukuyama
• CV of Fukuyama