Yoshinori Kamikubo

Efficient 1,8- and 1,9-asymmetric inductions in the Grignard reaction of δ- and ɛ-keto esters of 1,1′-binaphthalen-2-ols with an oligoether tether as the 2′-substituent: application to the synthesis of (−)-malyngolide

Masamitsu Date, Yasufumi Tamai, Tetsutaro Hattori et al. · Journal of the Chemical Society Perkin Transactions 1 · 2001 · 22 citations

Natural Sciences, Chemistry, Drug Discovery +12

Pseudo-macrocyclic chelation control in remote asymmetric induction. Highly efficient 1,7-asymmetric inductive hydride reduction and Grignard reaction of γ-keto esters of 1,1′-binaphthalen-2-ols bearing an appropriate oligoether group as the 2′-substituent

Yasufumi Tamai, Tetsutaro Hattori, Masamitsu Date et al. · Journal of the Chemical Society Perkin Transactions 1 · 1999 · 14 citations

Natural Sciences, Chemistry, Catalysis +11

Efficient 1,8- to 1,12-asymmetric induction in Grignard reactions of ω-keto esters by using BINOL or its 2′-oligoether derivatives as the chiral auxiliary

Yasufumi Tamai, Tetsutaro Hattori, Masamitsu Date et al. · Journal of the Chemical Society Perkin Transactions 1 · 1999 · 13 citations

Natural Sciences, Chemistry, Catalysis +9