[3 + 2]-Cycloadditions of Azomethine Imines and Ynolates
Author:
Affiliation:
1. Department of Biochemistry, Division of Chemistry, UT Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, Texas 75390-9038, United States
Funder
Welch Foundation
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.6b01104
Reference31 articles.
1. Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products
2. Asymmetric 1,3-Dipolar Cycloaddition Reactions
3. Syntheses by Means of 1-Alkylidene- and 1-(Arylalkylidene)-3-pyrazolidoneN,N-Betaines, a New Type of Stable Azomethine Imine
4. 1,3-Dipolar cycloadditions of azomethine imines
5. A New Copper-Catalyzed [3 + 2] Cycloaddition: Enantioselective Coupling of Terminal Alkynes with Azomethine Imines To Generate Five-Membered Nitrogen Heterocycles
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