Catalyst-free, aza-Michael polymerization of hydrazides: polymerizability, kinetics, and mechanistic origin of an α-effect
Author:
Affiliation:
1. Department of Chemical and Biological Engineering
2. University of Colorado Boulder
3. Boulder
4. USA
5. Department of Chemistry
6. Colorado School of Mines
7. Golden
8. Materials Science and Engineering Program
Abstract
α-Effect observed in unsubstituted hydrazide nucleophiles imbues highly efficient bis-addition reactivity in the aza-Michael reaction of hydrazides, in contrast to primary alkyl amines.
Funder
National Science Foundation
National Institutes of Health
U.S. Department of Education
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Polymers and Plastics,Biochemistry,Bioengineering
Link
http://pubs.rsc.org/en/content/articlepdf/2019/PY/C9PY01199D
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5. Assembly of nitrogen-containing heterocycles initiated by the aza-Michael reaction
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