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Stereoselective Total Synthesis of Ophiocerin C through Two Different Approaches
Author(s) -
Srilatha Malampati,
Das Biswanath
Publication year - 2014
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.201400086
Subject(s) - chemistry , stereoselectivity , sharpless asymmetric dihydroxylation , total synthesis , acetaldehyde , dihydroxylation , propylene oxide , stereochemistry , sharpless epoxidation , organic chemistry , enantioselective synthesis , catalysis , ethylene oxide , polymer , ethanol , copolymer
Stereoselective total synthesis of ophiocerin C has been accomplished through two different approaches starting separately from acetaldehyde and from ( R )‐propylene oxide, and Sharpless asymmetric dihydroxylation has been employed as the key step in both approaches.