Ab Initio Calculations of the Potential Surface for Rearrangement of 2,2,3,3-Tetrafluoromethylenecyclopropane to 1-(Difluoromethylene)-2,2-difluorocyclopropane-Reference-Cited by-同舟云学术

Ab Initio Calculations of the Potential Surface for Rearrangement of 2,2,3,3-Tetrafluoromethylenecyclopropane to 1-(Difluoromethylene)-2,2-difluorocyclopropane

Published:2006-12-01 Issue:51 Volume:128 Page:16676-16683
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Wei Haiyan¹,Hrovat David A.¹,Borden Weston Thatcher¹

Affiliation:

1. Contribution from the Department of Chemistry, University of North Texas, P.O. Box 305070, Denton, Texas 76203-5070

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja065963y

Reference39 articles.

1. Thermal rearrangements of gem-difluorocyclopropanes

2. Thermal isomerization and fragmentation of 1,1-difluoro-2,3-dimethylcyclopropane

3. Ab Initio Calculations on the Stereomutation of 1,1-Difluorocyclopropane. Prediction of a Substantial Preference for Coupled Disrotation of the Methylene Groups

4. Experimental Study of the Stereomutation of 1,1-Difluoro-2-ethyl-3-methylcyclopropane Confirms the Predicted Preference for Disrotatory Ring Opening and Closure

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