Out of cross-conjugation: the unexpected structure of tetrazinones-Reference-Cited by-同舟云学术

Out of cross-conjugation: the unexpected structure of tetrazinones

Published:2014 Issue:88 Volume:4 Page:47762-47768
ISSN:2046-2069
Container-title:RSC Adv.
language:en
Short-container-title:RSC Adv.

Author:

Bényei A. C.¹²³⁴,Stirling A.⁵⁶⁷⁸,Bostai B.⁹¹⁰⁸,Lőrincz K.⁹¹⁰⁸,Kotschy A.⁹¹⁰⁸

Affiliation:

1. Laboratory of X-ray Diffraction

2. Department of Pharmaceutical Chemistry

3. University of Debrecen

4. H-4010 Debrecen, Hungary

5. Institute of Organic Chemistry

6. Research Centre for Natural Sciences

7. Hungarian Academy of Sciences

8. H-1117 Budapest, Hungary

9. Institute of Chemistry

10. Eötvös Loránd University

Abstract

Combined experimental and theoretical investigations helped to elucidate the mechanisms responsible for the unique structural and electronic properties of NHC-substituted tetrazinone compounds.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/RA/C4RA05616G

Reference55 articles.

1. J. Sauer , 1,2,4,5-tetrazines, in Comprehensive Heterocyclic Chemistry, II, ed. A. J.Boulton, A. R.Katritzky, C. W.Rees and E. F.Scriven, Pergamon, New York, 1996, pp. 901–955

2. D. L. Boger and S. M.Weinreb, Hetero Diels–Alder methodology in organic synthesis, Academic, New York, 1997

3. 3,3′-Azobis(6-amino-1,2,4,5-tetrazine): A Novel High-Nitrogen Energetic Material

4. Novel High-Nitrogen Materials Based on Nitroguanyl-Substituted Tetrazines

5. “Green” Pyrotechnics: A Chemists' Challenge

Cited by 3 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

1. A new class of unique quinoidal-like imidazoliumyl tetrazinides: synthesis, structure, and mechanism;New Journal of Chemistry;2024

2. Head‐to‐Tail Dimerization of N‐Heterocyclic Diazoolefins;Angewandte Chemie;2023-05-09

3. Head‐to‐Tail Dimerization of N‐Heterocyclic Diazoolefins;Angewandte Chemie International Edition;2023-05-09