The O-Acylation of Ketone Enolates by Allyl 1H-Imidazole-1-carboxylate Mediated with Boron Trifluoride EtherateA Convenient Procedure for the Synthesis of Substituted Allyl Enol Carbonates-Reference-Cited by-同舟云学术

The O-Acylation of Ketone Enolates by Allyl 1H-Imidazole-1-carboxylate Mediated with Boron Trifluoride EtherateA Convenient Procedure for the Synthesis of Substituted Allyl Enol Carbonates

Published:2007-10-27 Issue:24 Volume:72 Page:9372-9375
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Trost Barry M.¹,Xu Jiayi¹

Affiliation:

1. Department of Chemistry, Stanford University, 337 Campus Drive, Stanford, California 94305-5080 bmtrost@stanford.edu

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo7016313

Reference23 articles.

1. An efficient synthesis of enol carbonates

2. Palladium-catalyzed allylation of ketones and aldehydes via allyl enol carbonates

3. C-Acylation of Enolates by Methyl Cyanoformate: An Examination of Site- and Stereoselectivity

4. Efficient preparation of enol carbonates by selective O-acylation of ketone sodium enolates generated in the presence of TMEDA

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