Direct Conversion of N-Methoxy-N-methylamides (Weinreb Amides) to Ketones via a Nonclassical Wittig Reaction-Reference-Cited by-同舟云学术

Direct Conversion of N-Methoxy-N-methylamides (Weinreb Amides) to Ketones via a Nonclassical Wittig Reaction

Published:2005-03-01 Issue:7 Volume:7 Page:1427-1429
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Murphy John A.¹,Commeureuc Aurélien G. J.¹,Snaddon Thomas N.¹,McGuire Thomas M.¹,Khan Tanweer A.¹,Hisler Kevin¹,Dewis Mark L.¹,Carling Robert¹

Affiliation:

1. Department of Pure and Applied Chemistry, University of Strathclyde, Thomas Graham Building, 295 Cathedral Street, Glasgow G1 1XL, U.K., International Flavors and Fragrances (IFF-R & D), 1515 State Highway 36, Union Beach, New Jersey 07735, and Merck, Sharp & Dohme Ltd., Neuroscience Research Centre, Terlings Park, Eastwick Road, Harlow, Essex CM20 2QR, U.K.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol050337b

Reference8 articles.

1. N-methoxy-n-methylamides as effective acylating agents

2. Addition of Metallo Enolates to Chiral 1-Acylpyridinium Salts: Total Synthesis of (+)-Cannabisativine

3. Substituted Oxocanes by Intramolecular Allylboration Reactions. Entry to an Efficient Synthesis of (+)-Laurencin

4. Acylation of ester enolates by N-methoxy-N-methylamides: an effective synthesis of .beta.-keto esters

5. Chemoselective Dieckmann-like condensations using N-methoxy-N-methylamides

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