Asymmetric Synthesis of Substituted 2-Azaspiro[3.5]nonan-1-ones: An Enantioselective Synthesis of the Cholesterol Absorption Inhibitor (+)-SCH 54016
- 15 November 1996
- journal article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 61 (23), 8341-8343
- https://doi.org/10.1021/jo961096b
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- Substituted 2-azaspiro[5.3]nonan-1-ones as potent cholesterol absorption inhibitors: defining a binding conformation for SCH 48461Journal of Medicinal Chemistry, 1995
- Stereoselective aldol reactions of chlorotitanium enolates. An efficient method for the assemblage of polypropionate-related synthonsJournal of the American Chemical Society, 1991
- Carbanions derived from 3-methoxyazetidinones: precursors for the preparation of 3,3-disubstituted azetidinonesThe Journal of Organic Chemistry, 1990
- Magnesium-methanol as a simple convenient reducing agent for α,β -unsaturated estersTetrahedron Letters, 1986
- An improved procedure for the two carbon homologation of esters to α, β-unsaturated estersTetrahedron Letters, 1986
- Mixed solvents containing methanol as useful reaction media for unique chemoselective reductions within lithium borohydrideThe Journal of Organic Chemistry, 1986
- Synthesis of Substituted Spiro[azetidin-2-one-4,2'(or 3,2')-tricyclo[3.3.1.13,7]decane] DerivativesHETEROCYCLES, 1986
- Photochemical synthesis of spiro-β-lactamsJournal of the Chemical Society, Chemical Communications, 1984
- Synthesis of difunctionalized iceane derivatives: 3,13-dimethylene-8-oxapentacyclo[8.3.1.12,6.04,12.06,10]pentadecaneJournal of the American Chemical Society, 1983
- Zur ReaktionsweiseN-metallierter 2-Azetidinon- und AzetidinderivateEuropean Journal of Organic Chemistry, 1976