Enantioselective total synthesis of ginkgolide derivatives lacking the tert-butyl group, an essential structural subunit for antagonism of platelet activating factor
- 31 December 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (36) , 4623-4626
- https://doi.org/10.1016/s0040-4039(00)92265-2
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Simple analogs of ginkgolide b which are highly active antagonists of platelet activating factorTetrahedron Letters, 1989
- Enantioselective route to a key intermediate in the total synthesis of ginkgolide BTetrahedron Letters, 1988
- Robert Robinson Lecture. Retrosynthetic thinking—essentials and examplesChemical Society Reviews, 1988
- A stable and easily prepared catalyst for the enantioselective reduction of ketones. Applications to multistep synthesesJournal of the American Chemical Society, 1987
- Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implicationsJournal of the American Chemical Society, 1987
- The Ginkgolides: Potent platelet-activating factor antagonists isolated from Ginkgo biloba L.. Chemistry, pharmacology and clinical applicationsDrugs of the Future, 1987