Syntheses, Thermal Reactivities, and Computational Studies of Aryl-Fused Quinoxalenediynes: Effect of Extended Benzannelation on Bergman Cyclization Energetics-Reference-Cited by-同舟云学术

Syntheses, Thermal Reactivities, and Computational Studies of Aryl-Fused Quinoxalenediynes: Effect of Extended Benzannelation on Bergman Cyclization Energetics

Published:2012-10-31 Issue:22 Volume:77 Page:10329-10339
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Spence John D.¹,Rios Andro C.¹,Frost Megan A.¹,McCutcheon Claire M.¹,Cox Christopher D.¹,Chavez Sonia¹,Fernandez Ramiro¹,Gherman Benjamin F.¹

Affiliation:

1. Department of Chemistry, California State University, Sacramento, Sacramento, California 95819, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo302009c

Reference101 articles.

1. p-Benzyne. Generation as an intermediate in a thermal isomerization reaction and trapping evidence for the 1,4-benzenediyl structure

2. Reactive 1,4-dehydroaromatics

3. Comparison of biradical formation between enediyne and enyne-allene. Ab initio CASSCF and MRSDCI study

4. A Valence Bond Study of the Bergman Cyclization: Geometric Features, Resonance Energy, and Nucleus-Independent Chemical Shift (NICS) Values

5. Reactant Destabilization in the Bergman Cyclization and Rational Design of Light- and pH-Activated Enediynes

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