Cutting-Edge and Time-Honored Strategies for Stereoselective Construction of C–N Bonds in Total Synthesis
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, University of California, Santa Barbara, California 93106, United States
2. Department of Chemistry, University of Science and Technology of China, 96 Jinzhai Road, Hefei, Anhui 230026, China
Funder
National Institute of Environmental Health Sciences
Division of Chemistry
National Institute of General Medical Sciences
National Science Foundation
Publisher
American Chemical Society (ACS)
Subject
General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.chemrev.5b00712
Reference824 articles.
1. Total Synthesis of (−)-Chamobtusin A
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4. Asymmetric syntheses of (–)-lentiginosine and an original pyrrolizidinic analogue thereof from a versatile epoxyamine intermediate
5. Total synthesis of calystegine A7
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