Formation of 5,6- and 7,8-dihydrohexahelicene: mechanistic details of the rearrangement of the primary photocyclization product of 2-styrylbenzo[c]phenanthrene in the presence of a base
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo00276a034
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
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2. Preparation and Physicochemical Properties of [6]Helicenes Fluorinated at Terminal Rings;The Journal of Organic Chemistry;2019-01-25
3. Synthesis, Structures, and Photophysical Properties of Optically Stable 1,16-Diphenyl-3,14-diaryl-Substituted Tetrahydrobenzo[5]helicenediol Derivatives: Enantioselective Recognition toward Tryptophan Methyl Esters;The Journal of Organic Chemistry;2017-07-07
4. Preparation of Phenanthrenes by Photocyclization of Stilbenes Containing a Tosyl Group on the Central Double Bond. A Versatile Approach to the Synthesis of Phenanthrenes and Phenanthrenoids;The Journal of Organic Chemistry;2010-09-13
5. The influence of the chiral environment in the photosynthesis of enantiomerically enriched hexahelicene. A sudden change in the chirality of hexahelicene by a change in the temperature of a chiral crystalline medium;Recueil des Travaux Chimiques des Pays-Bas;1995
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