Regioselective Reactions of Highly Substituted Arynes-Reference-Cited by-同舟云学术

Regioselective Reactions of Highly Substituted Arynes

Published:2010-02-18 Issue:6 Volume:12 Page:1224-1227
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Tadross Pamela M.¹,Gilmore Christopher D.¹,Bugga Pradeep¹,Virgil Scott C.¹,Stoltz Brian M.¹

Affiliation:

1. The Arnold and Mabel Beckman Laboratories of Chemical Synthesis, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol1000796

Reference27 articles.

1. Orientation, Reactivity, and Mechanism in the Addition of Methanol to 4-Chlorobenzyne1

2. Orientation and reactivity in nucleophilic addition to arynes possessing charged substituents. I. Orientation and reactivity in nucleophilic addition to benzyne-3- and -4-carboxylate

3. One Century of Aryne Chemistry

4. Influence of Hydroxyl Substitution on Benzyne Properties. Quantum Chemical Characterization of the Didehydrophenols

5. Substituent effects on the reactivity of arynes. Product distributions as an index of relative reactivities of arynes in methylamine and dimethylamine solvents

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