Decarboxylative Annulation of α-Amino Acids with γ-Nitroaldehydes
Author:
Affiliation:
1. Department of Chemistry and Chemical Biology, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854, United States
Funder
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.6b02020
Reference79 articles.
1. The Azomethine Ylide Route to Amine C–H Functionalization: Redox-Versions of Classic Reactions and a Pathway to New Transformations
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3. C–H functionalization of cyclic amines: redox-annulations with α,β-unsaturated carbonyl compounds
4. Intramolecular Redox-Mannich Reactions: Facile Access to the Tetrahydroprotoberberine Core
5. An Ugi Reaction Incorporating a Redox-Neutral Amine C–H Functionalization Step
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