Cross-Coupling of Primary Amides to Aryl and Heteroaryl Partners Using (DiMeIHeptCl)Pd Promoted by Trialkylboranes or B(C6F5)3-Reference-Cited by-同舟云学术

Cross-Coupling of Primary Amides to Aryl and Heteroaryl Partners Using (DiMeIHeptCl)Pd Promoted by Trialkylboranes or B(C6F5)3

Published:2017-12-15 Issue:51 Volume:139 Page:18436-18439
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Sharif Sepideh¹,Day Jonathan¹,Hunter Howard N.¹,Lu Yu²,Mitchell David²,Rodriguez Michael J.²,Organ Michael G.¹³^ORCID

Affiliation:

1. Department of Chemistry, York University 4700 Keele Street, Toronto M3J 1P3, Canada

2. Lilly Research Laboratories, a Division of Eli Lilly and Company, Indianapolis, Indiana 46285, United States

3. Centre for Catalysis Research and Innovation (CCRI) and Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa K1N6N5, Canada

Funder

Natural Sciences and Engineering Research Council of Canada

Eli Lilly and Company

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.7b09488

Reference29 articles.

1. Prodrugs for Amines

2. Rethinking amide bond synthesis

3. Synthesis studies directed toward gelsemine. Preparation of an advanced pentacyclic intermediate

4. Palladium-Catalyzed Intermolecular Coupling of Aryl Halides and Amides

5. Applications of Palladium-Catalyzed C–N Cross-Coupling Reactions

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