Enantiospecific Aluminum-Catalyzed (3+2) Cycloaddition of Unactivated Aziridines with Isothiocyanates
Author:
Affiliation:
1. Department of Chemistry, Indian Institute of Technology Guwahati, Guwahati 781039, India
2. Department Chemistry, Graduate School of Science and Technology, Kumamoto University, 2-39-1 Kurokami, Chuo-ku, Kumamoto 860-8555, Japan
Funder
University Grants Commission
Department of Science and Technology, Ministry of Science and Technology
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.6b02190
Reference34 articles.
1. Aziridines in Formal [3+2] Cycloadditions: Synthesis of Five-Membered Heterocycles
2. Room Temperature Ring-Opening Cyclization Reactions of 2-Vinylaziridines with Isocyanates, Carbodiimides, and Isothiocyanates Catalyzed by [Pd(OAc)2]/PPh3
3. Dynamic Kinetic Asymmetric Cycloadditions of Isocyanates to Vinylaziridines
4. Construction of Linked Nitrogen Heterocycles by Palladium(0)-Catalyzed Intramolecular Domino Cyclization of 2-Alkynylaziridines Bearing a 2-Aminoethyl Group via Ring Expansion with Isocyanate
5. Synthesis of 2-Oxazoline-2-amines and 2-Thiazoline-2-amines by Reaction of Aziridinium Tetrafluoroborate with Isocyanates and Isothiocyanates
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