Base-switched annuloselectivity in the reactions of ethyl malonyl chloride and imines
Author:
Affiliation:
1. State Key Laboratory of Chemical Resource Engineering
2. Department of Organic Chemistry
3. Faculty of Science
4. Beijing University of Chemical Technology
5. Beijing 100029, P. R. China
Abstract
The [2 + 2] and [2 + 2 + 2] annuloselectivity in the reactions of ethyl malonyl chloride with imines was controlled by different bases, providing a simple synthesis of β-lactam-3-carboxylates and 2,3-dihydro-1,3-oxazin-4-ones.
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2014/OB/C4OB01454E
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