Ring-fused hexahydro-1,2,4,5-tetrazines: synthesis, structure, and mechanistic studies on isolable rotational isomers
-
Published:2023
Issue:6
Volume:59
Page:700-703
-
ISSN:1359-7345
-
Container-title:Chemical Communications
-
language:en
-
Short-container-title:Chem. Commun.
Author:
Toda Yasunori1ORCID,
Kooguchi Airi1,
Sukegawa Kimiya1,
Kikuchi Ayaka1,
Suga Hiroyuki1ORCID
Affiliation:
1. Department of Materials Chemistry, Faculty of Engineering, Shinshu University, 4-17-1, Wakasato, Nagano, 380-8553, Japan
Abstract
Here, we report the design and synthesis of isolable rotational isomers with a hexahydro-1,2,4,5-tetrazine core. The mechanism of the isomerization via a twist-boat conformation was elucidated by DFT calculations.
Funder
Japan Society for the Promotion of Science
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis
Reference44 articles.
1. Unusually High Barriers to Rotation Involving the Tetrahedral Carbon Atom
2. M.Ōki , Recent Advances in Atropisomerism. In Topics in Stereochemistry , N. L. Allinger , E. L. Eliel and S. H. Wilen , ed., John Wiley & Sons , 1983 , ch. 1, pp. 1–81
3. M.Ōki , The Chemistry of Rotational Isomers , Springer , 1993
4. E. L.Eliel and S. H.Wilen , Stereochemistry of Organic Compounds , Wiley-Interscience , New York , 1994
5. Atroposelective Synthesis of Axially Chiral Biaryl Compounds
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献