De novo Assembly of the Benzenoid Ring as a Core Strategy for Synthesis of the Isoindolinone Natural Products Isohericerin, Erinacerin A, and Sterenin A
Author:
Affiliation:
1. Department of Chemistry, University of Minnesota, 207 Pleasant Street SE, Minneapolis, Minnesota 55455, United States
Funder
U.S. Department of Health and Human Services
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c02752
Reference50 articles.
1. 1-Isoindolinone scaffold-based natural products with a promising diverse bioactivity
2. Reductive Coupling of Phthalimides with Ketones and Aldehydes by Low-Valent Titanium: One-Pot Synthesis of Alkylideneisoindolin-1-ones
3. Organic Synthesis Methodology. Preparation and Diastereoselective Birch Reduction−Alkylation of 3-Substituted 2-Methyl-2,3-dihydroisoindol-1-ones
4. A new simple and convenient synthesis of 3-substituted phthalimidines
5. Combining α-amidoalkylation reactions of N-acyliminium ions with ring-closing metathesis: access to versatile novel isoindolones spirocyclic compounds
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