Highly Diastereoselective Synthesis of γ-Lactams Enabled by Photoinduced Deaminative [3 + 2] Annulation Reaction
Author:
Affiliation:
1. State Key Lab of Urban Water Resource and Environment, School of Science, Harbin Institute of Technology, Shenzhen, Guangdong 518055, China
2. School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang, Henan 453007, China
Funder
Guangdong Science and Technology Department
Government of Guangdong Province
Henan Normal University
Science, Technology and Innovation Commission of Shenzhen Municipality
National Natural Science Foundation of China
Natural Science Foundation of Guangdong Province
Shenzhen Government
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c01565
Reference58 articles.
1. Biologically active γ-lactams: synthesis and natural sources
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3. Radical Cyclization of 1, n ‐Enynes and 1, n ‐Dienes for the Synthesis of 2‐Pyrrolidone
4. Multistep continuous-flow synthesis of (R)- and (S)-rolipram using heterogeneous catalysts
5. Rolipram Protects Mice from Gram-negative Bacterium Escherichia coli-induced Inflammation and Septic Shock
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