Covalent modification of biological targets with natural products through Paal–Knorr pyrrole formation
Author:
Affiliation:
1. Department of Chemistry and Biochemistry
2. Texas State University
3. San Marcos
4. USA
5. University of California at San Diego
6. Xenobe Research Institute
7. San Diego
Abstract
This review examines the extent to which natural systems have adopted the Paal–Knorr reaction to engage nucleophilic amine groups within biological targets.
Funder
National Cancer Institute
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2017/NP/C7NP00024C
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