| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5279780 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
Methods have been developed for the regioselective formation of both aldol condensation products from a non-symmetrical dialdehyde derived from 5α-cholestan-3-one. The findings disclosed herein, as well as their mechanistic implications, should assist in achieving selective intramolecular aldol closures in other contexts.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Scott A. Snyder, E.J. Corey,