Chemical Communications p. 2705 - 2706 (1996)
Update date:2022-08-17
Topics:
Tanaka, Hideo
Yamaguchi, Yoshihiko
Sumida, Shin-Ichi
Torii, Sigeru
A sequential reductive 1,2-elimination and hydride addition process for 3,4-disubstituted butenoates derived from penicillin is successfully performed with the aid of a combination of tributyltin hydride and copper(I) chloride in N-methyl-2-pyrrolidinone
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