Reactivity and Stereoselectivity of 6π and Nazarov Electrocyclizations of Bridged Bicyclic Trienes and Divinyl Ketones
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095, United States
2. Department of Chemistry, University of Alberta, Edmonton, AB T6G 2G2, Canada
Funder
Division of Chemistry
University of California, Los Angeles
Natural Sciences and Engineering Research Council of Canada
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.5b00070
Reference54 articles.
1. Highly Stereoselective 6π Electrocyclization of Bridged Bicyclic 1,3,5-Trienes
2. Stereoselective Nazarov Cyclizations of Bridged Bicyclic Dienones
3. Unexpected Participation of an Unconjugated Olefin during Nazarov Cyclization of Bridged Bicyclic Dienones
4. Transition Structures of the Electrocyclic Reactions ofcis,cis,cis-1,3,5-Cyclooctatriene
5. Transition Structures of Thermally Allowed Disrotatory Electrocyclizations. The Prediction of Stereoselective Substituent Effects in Six-Electron Pericyclic Reactions
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