Dramatic Acceleration of the Pd-Catalyzed [4+2] Benzannulation Reaction of Enynes and Diynes in the Presence of Lewis Acids and Bases: Expanded Scope and New Mechanistic Insights-Reference-Cited by-同舟云学术

Dramatic Acceleration of the Pd-Catalyzed [4+2] Benzannulation Reaction of Enynes and Diynes in the Presence of Lewis Acids and Bases: Expanded Scope and New Mechanistic Insights

Published:2006-04-07 Issue:17 Volume:128 Page:5818-5827
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Rubina Marina¹,Conley Matthew¹,Gevorgyan Vladimir¹

Affiliation:

1. Contribution from the Department of Chemistry, University of Illinois at Chicago, 845 West Taylor Street, Chicago, Illinois 60607-7061

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja060085p

Reference33 articles.

1. A New Palladium-Catalyzed Benzannulation of Conjugated Enynes

2. Pd-Catalyzed One-Pot Multicomponent Coupling Reaction for the Highly Regioselective Synthesis of Polysubstituted Benzenes

3. Stannylative Cycloaddition of Enynes Catalyzed by Palladium−Iminophosphine

4. Intramolecular [4+2] Cycloaddition Reactions of Conjugated Enynes

5. Regiospesific Synthesis of Polysubstituted Phenols via the Palladium-Catalyzed Enyne−Diyne [4 + 2] Cross-Benzannulation Pathway

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