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Stereoselective synthesis of (+)-hyptolide
- 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 :
- *LACTONES
*METATHESIS reactions
Subjects
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