X-ray Crystal Structures and ab Initio Calculations on the Photochemically Formed Dewar Isomers of the 4(3H)-Pyrimidinone Derivatives-Reference-Cited by-同舟云学术

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X-ray Crystal Structures and ab Initio Calculations on the Photochemically Formed Dewar Isomers of the 4(3H)-Pyrimidinone Derivatives

Published:1997-05-01 Issue:9 Volume:62 Page:2711-2719
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Hirokami Shun-ichi¹,Murao Akihiro¹,Kakuda Hiroko¹,Shinoda Hiroyuki²,Koga Yoshinori³

Affiliation:

1. Laboratory of Chemistry, Toyama Medical and Pharmaceutical University, Sugitani 2630, Toyama 930-01, Japan

2. Faculty of Pharmaceutical Sciences, Toyama Medical and Pharmaceutical University, Sugitani 2630, Toyama 930-01, Japan

3. Department of Advanced Chemical Technology, National Institute of Materials and Chemical Research, 1-1, Higashi, Tsukuba, Ibaraki 305, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo962103z

Reference48 articles.

1. Photochemical reactions of 4-pyrimidones. Structures and properties of the .beta.-lactams formed

2. Photochemistry of 2,3,6-trialkyl-4-pyrimidinones in liquid ammonia-ether solution. Chemistry of Dewar 4-pyrimidinones

3. New general synthesis of diaryl tellurides from aromatic amines

4. Photochemical reactions of 4-pyrimidinones in acetic acid. Formation of 5-carboxypyrimidinium betaines

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1. Lewis Acid-Promoted Ring-Contraction of 2,4,6,8-Tetrasubstituted 1,5-Diazacyclooctatetraenes to 2,4,6-Trisubstituted Pyridines;Organic Letters;2018-01-05

2. Solid H2versus solid noble-gas environment: Influence on photoinduced hydrogen-atom transfer in matrix-isolated 4(3H)-pyrimidinone;The Journal of Chemical Physics;2017-03-07

3. ChemInform Abstract: X-Ray Crystal Structures and ab initio Calculations on Photochemically Formed Dewar Isomers of Type (I) of 4(3H)-Pyrimidinone Derivatives.;ChemInform;2010-08-03

4. Azetidines, Azetines and Azetes: Monocyclic;Comprehensive Heterocyclic Chemistry III;2008

5. Molecular Modeling of Anti-Bredt Compounds;Journal of Chemical Information and Modeling;2005-02-02

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