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Stereoselective synthesis of (+)-hyptolide

Authors :
Murga, Juan
Garcıa-Fortanet, Jorge
Carda, Miguel
Marco, J. Alberto
Source :
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry. Feb2003, Vol. 44 Issue 9, p1737. 3p.
Publication Year :
2003

Abstract

The first total synthesis of the naturally occurring lactone (+)-hyptolide is described. Ethyl l-lactate was the chiral starting material. Key steps of this 15-step synthesis were a Brown''s asymmetric allylation, a Carreira''s asymmetric ethynylation and a ring closing metathesis. [Copyright &y& Elsevier]

Subjects

Subjects :
*LACTONES
*METATHESIS reactions

Details

Language :
English
ISSN :
00404039
Volume :
44
Issue :
9
Database :
Academic Search Index
Journal :
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry
Publication Type :
Academic Journal
Accession number :
9050760
Full Text :
https://doi.org/10.1016/S0040-4039(03)00125-4