Total synthesis of forskolin — Part III studies related to an asymmetric synthesis
Authors:
- Daniel CalvoDCDaniel Calvo
- Marc PortMPMarc Port
- Bernard DelpechBDBernard Delpech
- Robert LettRLRobert Lett
- 1 February 1996
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 37 (7) , 1023-1024
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- A synthesis of an optically active forskolin intermediate via allenyl ether intramolecular cycloaddition strategyTetrahedron: Asymmetry, 1990
- A short and efficient enantioselective route to a key intermediate for the total synthesis of forskolinTetrahedron Letters, 1989
- An efficient synthesis of a key intermediate of forskolinJournal of the Chemical Society, Chemical Communications, 1989
- Total synthesis of (.+-.)-forskolinJournal of the American Chemical Society, 1988
- A total synthesis of (.+-.)-forskolinJournal of the American Chemical Society, 1988
- Formation of (±)-forskolin via a cuprate addition to a synthetic dihydropyran-4-oneTetrahedron Letters, 1988
- Enantioselective route to a key intermediate in the total synthesis of forskolinTetrahedron Letters, 1988
- A synthetic route to forskolinJournal of the American Chemical Society, 1987
- Reconstitution of forskolin from a ring C dihydropyran-4-one degradation product thereofTetrahedron Letters, 1987
- A C6, C7 Oxygen Functionalized Intermediate for the Synthesis of Forskolin: Stereochemical Control in an Intramolecular Diels-Alder ReactionTetrahedron Letters, 1985