936716-29-9Relevant academic research and scientific papers
Concise stereoselective total synthesis of (4 R, 6 R)-lactone moiety analog of mevinoline and compactin
Rao, D. Chandra,Reddy, D. Kumar,Chinnababu,Shekhar,Venkateswarlu
supporting information, p. 2980 - 2984 (2013/09/12)
A simple and highly efficient synthetic route has been developed for analogue of HMGCo A reductase inhibitor (1). The strategy utilizes S-Corey-Bakshi-Shibata (CBS) reduction, FeCl3-catalyzed C-H insertion of ethyl diazoacetate.
Stereoselective synthesis of a mevinic acid analogue
Sabitha, Gowravaram,Sudhakar,Srinivas,Yadav
, p. 705 - 708 (2007/12/29)
An efficient and versatile synthetic method for the stereoselective synthesis of a mevinic acid analogue is described. This approach uses a combination of a Cosford protocol with a catecholborane-mediated stereoselective reduction of acyclic P-hydroxy ket
