Abstract
An efficient and straightforward stereoselective alkylation reaction of enamides using commercially available and easily accessible unactivated alkyl carboxylic acids as alkylating agents is described, giving rise to a diverse array of synthetically important and geometrically defined β-alkylated enamides bearing primary, secondary, or tertiary alkyl moieties. This transformation also shows excellent functional group tolerance, satisfying atom economy, and operational simplicity.
Original language | English |
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Pages (from-to) | 8395-8399 |
Number of pages | 5 |
Journal | Organic Letters |
Volume | 21 |
Issue number | 20 |
DOIs | |
Publication status | Published - Oct 18 2019 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:Copyright © 2019 American Chemical Society.
ASJC Scopus Subject Areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry