Ab Initio Study on the Keto−Enol Tautomerism of the α-Substituted Acetaldehydes XH2CCHO (X = H, BH2, CH3, NH2, OH, F, CN, NC, and Cl): Comparison with the Tautomerism in α-Substituted Acetaldimines and Acetyl Derivatives-Reference-Cited by-同舟云学术

Ab Initio Study on the Keto−Enol Tautomerism of the α-Substituted Acetaldehydes XH2CCHO (X = H, BH2, CH3, NH2, OH, F, CN, NC, and Cl): Comparison with the Tautomerism in α-Substituted Acetaldimines and Acetyl Derivatives

Published:1999-04-01 Issue:17 Volume:103 Page:3289-3293
ISSN:1089-5639
Container-title:The Journal of Physical Chemistry A
language:en
Short-container-title:J. Phys. Chem. A

Author:

Su Chien-Chih¹,Lin Chao-Kuo¹,Wu Chen-Chang¹,Lien Min-Hsiung¹

Affiliation:

1. Department of Chemistry, National Chung Hsing University, Taichung 40227, Taiwan, Republic of China

Publisher

American Chemical Society (ACS)

Subject

Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jp9839910

Reference50 articles.

1. The Carbon–Nitrogen Triad Prototropic Tautomerism

2. Generation of simple enols in solution

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