Halo-Enediynes: Probing the Electronic and Stereoelectronic Contributions to the Bergman Cycloaromatization
Author:
Affiliation:
1. Department of Chemistry, Northeastern University, Boston, Massachusetts 02115
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo025763e
Reference26 articles.
1. DNA-damaging Enediyne Compounds
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3. Synthetic and mechanistic studies on esperamicin A1 and calichemicin .gamma.1. Molecular strain rather than .pi.-bond proximity determines the cycloaromatization rates of bicyclo[7.3.1]enediynes
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