221378-41-2Relevant academic research and scientific papers
Enzymatic desymmetrization of meso cis,cis-2,4,6-substituted tetrahydropyrans
Chenevert, Robert,Goupil, Daniel,Yannick, Stephane Rose,Bedard, Emmanuelle
, p. 4285 - 4288 (2007/10/03)
The stereoselective acylation of meso-tetrahydropyrans 6 and 7 by enol esters (vinyl acetate or isopropenyl acetate) in the presence of Candida antarctica lipase in organic media gave the corresponding (2R,4S,6S)- monoesters 10 and 11 in high enantiomeric purity. The hydrolysis of the corresponding diacetate derivatives 8 and 9 in the presence of the same enzyme provided the opposite enantiomers, (2S,4R,6R)-monoesters 10 and 11.
