187334-62-9Relevant academic research and scientific papers
Asymmetric synthesis of the δ-lactone moiety in mevinic acid derivatives using an enzymatic procedure
Kaku, Hidetaka,Tanaka, Masakazu,Norimine, Yoshihiko,Miyashita, Yuko,Suemune, Hiroshi,Sakai, Kiyoshi
, p. 195 - 201 (1997)
Asymmetric induction into meso-1,3-diacetoxy-5-cycloheptene 4 by PFL-catalyzed hydrolysis afforded monoacetate (1S,3R)-5 of 96% enantiomeric excess (e.e.), which was converted into a synthetic equivalent 14 of the δ-lactone moiety in mevinic acid derivatives.
