Enantioselective route to a key intermediate in the total synthesis of forskolin
- 31 December 1988
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 29 (49), 6409-6412
- https://doi.org/10.1016/s0040-4039(00)82359-x
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
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- Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implicationsJournal of the American Chemical Society, 1987
- Chapter 29. Forskolin and Adenylate Cyclase: New Opportunities in Drug DesignPublished by Elsevier ,1984
- Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) estersJournal of the American Chemical Society, 1973