Conformational Specificity in Photoinduced Intramolecular 1,7-Hydrogen Abstraction of Homonaphthoquinones with a Spiro-Linked Dibenzocycloheptene Ring
Author:
Affiliation:
1. Department of Applied Chemistry, Faculty of Engineering, Osaka University, Toyonaka, Osaka 560-0043, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol005520d
Reference32 articles.
1. (a) Wagner, P. J.; Park, B.S. InOrganic Photochemistry; Padwa, A., Ed.; Marcel Dekker, Inc. New York, 1991; Volume 11, Chapter 4, p 227.
2. Type II photoelimination and photocyclization of ketones
3. Conformational flexibility and photochemistry
4. Transition structures for intramolecular hydrogen-atom transfers: the energetic advantage of seven-membered over six-membered transition structures
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2. Conformational analysis in the reversible intramolecular [2+2] photocycloaddition of diphenylbicyclo[4.2.0]oct-3-ene-2,5-diones;Tetrahedron Letters;2006-11
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