Published January 20, 2005
| Supplemental Material
Journal Article
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Chemoselective Construction of Substituted Conjugated Dienes Using an Olefin Cross-Metathesis Protocol
Abstract
Various substituted conjugated dienes have been made by olefin cross-metathesis. Using either electronic or steric "protection," one of the olefins of the conjugated diene was deactivated relative to the other for cross-metathesis. The reactions proceed with very high chemoselectivity and, when steric deactivation is used, very high diastereoselectivity.
Additional Information
© 2005 American Chemical Society. Received 7 October 2004. Published online 22 December 2004. Published in print 1 January 2005. This work was supported by a research grant from the National Institutes of Health.Attached Files
Supplemental Material - ol047929zsi20041007_115810.pdf
Supplemental Material - ol047929zsi20041012_052027.pdf
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Additional details
- Eprint ID
- 79384
- DOI
- 10.1021/ol047929z
- Resolver ID
- CaltechAUTHORS:20170726-074601198
- NIH
- Created
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2017-07-26Created from EPrint's datestamp field
- Updated
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2021-11-15Created from EPrint's last_modified field