Mori-Matsui synthesis

Mori, K., M. Ohki, K. Okada, Y. Takei, and M. Matsui Synthesis of [Pg.1447]

Full paper Mori, K. Matsui. "Synthesis of Compounds with Juvenile Hormone Activity-1. c//-Juvabione (Methyl c//-Todomatuate)" Tetrahedron 1968, 24, 3127-3138. 

Shiozaki, M., K. Mori, and M. Matsui Synthesis of Isocoumarins III Oosponol Diacetate. Agric. Biol. Chem. 32, 42 (1968). 

Mori, K., M. Uchida, and M. Matsui Synthesis of aliphatic insect pheromones from alicyclic starting materials (Z)-6-heneicosen-ll-one and (Z)-8-dodecenyl acetate. Tetrahedron 33, 385—387 (1977). 

Mori, K. Matsui, M. Diterpenoid total synthesis. XIII. Taxodione, a quinone methide tumor inhibitor. Tetrahedron 1970, 26, 3467-3473. 

In 1971, Mori, Saeki, and Matsui converted (185) the tricyclic acid 399, during their synthesis of kaur-16-en-19-oic acid (400), into the tetracyclic lactam 404 by the well-established photolytic method (186). The lactam 404 has previously been converted to veatchine and garryine by Wiesner s group. 

Ayyar and Rao (1967), and Mori and Matsui (1967) synthesised both compounds. The stereoselective synthesis was solved by Birch et al. (1969). 

Mori K, Matsui J, Yokota T, Sakai H, Bando M, Takeuchi Y (1999) Structure and synthesis of orobanchol, the germination stimulant for Orobanche minor. Tetrahedron Lett 40 943-946... 

Mori, K. Matsui, M. "Synthesis of d/-Juvabione (Methyi c//-Todomatuate), A Sesquiterpene Ester with Juveniie Hormone Activity" Tetrahedron Lett. 1967, 2515-2518. 

Juvabione synthesis K. Mori and M. Matsui Juvabione synthesis K. S. Ayyar and G. S. K. Rao Retrosynthetic analysis of juvabione with disconnection to a terpene structure... 

Mori, K., N. Mizumachi, and M. Matsui Pheromone synthesis. 12. Synthesis of optically pure (15, 45, 55)-2-pinen-4-ol (c/5-verbenol), the pheromone of Ips bark beetles. Agric. Biol. Chem. 40, 1611—1615 (1975). 

Mori, K., T. Takigawa, and M. Matsui Stereoselective synthesis of optically active disparlure, the pheromone of the gypsy moth (Porthetria dispar L.j. Tetrahedron Lett. 1976, 3953—3956. 

Mori, K., S. Tamada, and M. Matsui Stereocontrolled synthesis of the four possible stereoisomers of 6 ry / ro-3,7-dimethylpentadec-2-yl acetate and propionate, the sex pheromone of the pine sawflies. Tetrahedron Letters 1978, 901—904. 

Shiozaki, M., Mori, K., Matsui, M., and Hiroka, T, Photochemical synthesis of compounds with grayanotoxin skeleton. Tetrahedron Lett., 657, 1972. 

Mori, K., and M. Matsui Diterpenoid Total Synthesis-VIII ( )-Kaur-16-en-19-oic Acid, ( )-Kaur-16-en-19-ol, ( )-Monogynol, and Some Oxygenated Kauranes. Tetrahedron 24, 3095 (1968). 

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