Asymmetric synthesis with .alpha.,.beta.-bis[(methoxymethyl)oxy] ketones. Enantioselective total synthesis of natural (+)-indolizidine 195B (bicyclic gephyrotoxin 195B) and (-)-pinidine and their enantiomers from a common chiral synthon
- 1 February 1989
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 111 (4) , 1396-1408
- https://doi.org/10.1021/ja00186a038
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- An efficient, fully stereocontrolled total synthesis of N-benzoyl-L-daunosamineThe Journal of Organic Chemistry, 1986
- Highly selective total synthesis of enantiomerically pure (-)-anisomycinThe Journal of Organic Chemistry, 1986
- Alkaloids from dendrobatid poison frogs: trans-decahydroquinolines and indolizidinesTetrahedron, 1986
- Oxidation of long-chain and related alcohols to carbonyls by dimethyl sulfoxide "activated" by oxalyl chlorideThe Journal of Organic Chemistry, 1978
- The stereochemistry of pinidineTetrahedron, 1965
- Pinus Alkaloids. The Alkaloids of P. sabiniana Dougl. and Related SpeciesJournal of the American Chemical Society, 1955