Application of 6,7-Indole Aryne Cycloaddition and Pd(0)-Catalyzed Suzuki–Miyaura and Buchwald–Hartwig Cross-Coupling Reactions for the Preparation of Annulated Indole Libraries-Reference-Cited by-同舟云学术

Application of 6,7-Indole Aryne Cycloaddition and Pd(0)-Catalyzed Suzuki–Miyaura and Buchwald–Hartwig Cross-Coupling Reactions for the Preparation of Annulated Indole Libraries

Published:2011-06-30 Issue:5 Volume:13 Page:443-448
ISSN:2156-8952
Container-title:ACS Combinatorial Science
language:en
Short-container-title:ACS Comb. Sci.

Author:

Thornton Paul D.¹,Brown Neil²¹,Hill David¹,Neuenswander Ben¹,Lushington Gerald H.¹,Santini Conrad¹,Buszek Keith R.²¹

Affiliation:

1. Center of Excellence in Chemical Methodologies and Library Development, University of Kansas, 2034 Becker Drive, Lawrence, Kansas 66047, United States

2. Department of Chemistry, University of Missouri, 5100 Rockhill Road, Kansas City, Missouri 64110, United States

Publisher

American Chemical Society (ACS)

Subject

General Chemistry,General Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/co2000289

Reference35 articles.

1. Indole-Derived Arynes and Their Diels−Alder Reactivity with Furans

2. Concise Total Synthesis of (±)-cis-Trikentrin A and (±)-Herbindole A via Intermolecular Indole Aryne Cycloaddition

3. Regioselective Diels–Alder cycloadditions and other reactions of 4,5-, 5,6-, and 6,7-indole arynes

4. New synthesis of (±)-cis-trikentrin A via tandem indole aryne cycloaddition/Negishi reaction. Applications to library development

5. Experimental and Theoretical Investigations into the Unusual Regioselectivity of 4,5-, 5,6-, and 6,7-Indole Aryne Cycloadditions

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