Control of regioselectivity in the di-.pi.-methane rearrangements. Triplet-sensitized photoisomerization of benzonorbornadienes carrying cyano substituents in the aryl and vinyl segments-Reference-Cited by-同舟云学术

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Control of regioselectivity in the di-.pi.-methane rearrangements. Triplet-sensitized photoisomerization of benzonorbornadienes carrying cyano substituents in the aryl and vinyl segments

Published:1979-09 Issue:20 Volume:101 Page:5972-5980
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Paquette Leo A.,Ku Audrey Yeh,Santiago Cielo,Rozeboom Melvin D.,Houk K. N.

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja00514a017

Cited by 34 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

1. Substituent effect on di-π-methane reactions of benzopyrazinobarrelenes and benzoquinoxalinobarrelenes;Tetrahedron;2016-03

2. Substituent effects on the photorearrangements of unsymmetrically substituted diazinobarrelenes;RSC Adv.;2013

3. Di-Π-Methane Rearrangement;Comprehensive Organic Name Reactions and Reagents;2010-09-15

4. Ring Contraction of Bridgehead Sultams by Photoinduced Di-π-methane Rearrangement;The Journal of Organic Chemistry;2006-02-17

5. Proximitätseffekte in der Organischen Chemie - Die photoelektronenspektroskopische Untersuchung nichtbindender und transanularer Wechselwirkungen;Angewandte Chemie;2006-01-17

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