Ab Initio Study of the Substituent Effects on the Relative Stability of the E and Z Conformers of Phenyl Esters. Stereoelectronic Effects on the Reactivity of the Carbonyl Group-Reference-Cited by-同舟云学术

Ab Initio Study of the Substituent Effects on the Relative Stability of the E and Z Conformers of Phenyl Esters. Stereoelectronic Effects on the Reactivity of the Carbonyl Group

Published:2005-06-28 Issue:28 Volume:109 Page:6279-6289
ISSN:1089-5639
Container-title:The Journal of Physical Chemistry A
language:en
Short-container-title:J. Phys. Chem. A

Author:

Neuvonen Helmi¹,Neuvonen Kari¹,Koch Andreas¹,Kleinpeter Erich¹

Affiliation:

1. Department of Chemistry, University of Turku, FIN-20014 Turku, Finland, and University of Potsdam, D-14415 Potsdam, POB 691553, Germany

Publisher

American Chemical Society (ACS)

Subject

Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jp044172k

Reference36 articles.

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4. Theoretical elucidation of the origin of the anomalously high acidity of Meldrum's acid

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