Enantioselective Synthesis of the Alcohol Moiety of Dolabriferol
摘要:
Dolabriferol is a marine polypropionate characterized by an unusual noncontiguous carbon backbone. The two polypropionate subunits are linked by an ester function. The protected alcohol moiety of dolabriferol was synthesized via the enzymatic desymmetrization of meso-(anti-anti)-2,4-dimethyl-1,3,5-pentanetriol.
Enantioselective Synthesis of the Alcohol Moiety of Dolabriferol
摘要:
Dolabriferol is a marine polypropionate characterized by an unusual noncontiguous carbon backbone. The two polypropionate subunits are linked by an ester function. The protected alcohol moiety of dolabriferol was synthesized via the enzymatic desymmetrization of meso-(anti-anti)-2,4-dimethyl-1,3,5-pentanetriol.
Enantioselective Synthesis of the Alcohol Moiety of Dolabriferol
作者:Nicholas Pelchat、Dave Caron、Robert Chênevert
DOI:10.1021/jo701524p
日期:2007.10.1
Dolabriferol is a marine polypropionate characterized by an unusual noncontiguous carbon backbone. The two polypropionate subunits are linked by an ester function. The protected alcohol moiety of dolabriferol was synthesized via the enzymatic desymmetrization of meso-(anti-anti)-2,4-dimethyl-1,3,5-pentanetriol.