Reactions of Sterically Congested 1,5-Hexadienes: Ab Initio and DFT Calculations on the Competition between Cope Rearrangements and Disrotatory Cyclobutene Ring-Opening Reactions of Bridged syn-Tricyclo[4.2.0.02,5]octa-3,7-dienes-Reference-Cited by-同舟云学术

Reactions of Sterically Congested 1,5-Hexadienes: Ab Initio and DFT Calculations on the Competition between Cope Rearrangements and Disrotatory Cyclobutene Ring-Opening Reactions of Bridged syn-Tricyclo[4.2.0.02,5]octa-3,7-dienes

Published:2004-04-16 Issue:10 Volume:69 Page:3294-3301
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Bethke Sabine¹,Hrovat David A.¹,Borden Weston Thatcher¹,Gleiter Rolf¹

Affiliation:

1. Organisch-Chemisches Institut der Universität Heidelberg, Im Neuenheimer Feld 270, D-69120 Heidelberg, Germany, and Department of Chemistry, University of Washington, Box 351700, Seattle, Washington 98195-1700

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo030349f

Reference39 articles.

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4. Pericyclic Reaction Transition States: Passions and Punctilios, 1935-1995

5. Quantum Mechanical Methods and the Interpretation and Prediction of Pericyclic Reaction Mechanisms

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