Remarkable Synthesis of 2-(Z)-6-(E)-4H-[1,4]-Thiazepin-5-ones by Zwitterionic Rhodium-Catalyzed Chemo- and Regioselective Cyclohydrocarbonylative Ring Expansion of Acetylenic Thiazoles-Reference-Cited by-同舟云学术

Remarkable Synthesis of 2-(Z)-6-(E)-4H-[1,4]-Thiazepin-5-ones by Zwitterionic Rhodium-Catalyzed Chemo- and Regioselective Cyclohydrocarbonylative Ring Expansion of Acetylenic Thiazoles

Published:2001-01-17 Issue:6 Volume:123 Page:1017-1022
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Van den Hoven Bernard G.¹,Alper Howard¹

Affiliation:

1. Contribution from the Centre for Catalysis Research and Innovation, Department of Chemistry, University of Ottawa, 10 Marie Curie St., Ottawa, Ontario, Canada K1N 6N5

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja003085c

Reference45 articles.

1. Design and Synthesis of Potent Bradykinin Agonists Containing a Benzothiazepine Moiety

2. Synthesis and Characterization of Bradykinin B2 Receptor Agonists Containing Constrained Dipeptide Mimics

3. Dual Metalloprotease Inhibitors: Mercaptoacetyl-Based Fused Heterocyclic Dipeptide Mimetics as Inhibitors of Angiotensin-Converting Enzyme and Neutral Endopeptidase

4. In Vitro and In Vivo Effects of R023–6152 on Heart Mitochondrial Calcium and Energy Metabolism

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