Understanding the Activity and Enantioselectivity of Acetyl-Protected Aminoethyl Quinoline Ligands in Palladium-Catalyzed β-C(sp3)–H Bond Arylation Reactions-Reference-Cited by-同舟云学术

Understanding the Activity and Enantioselectivity of Acetyl-Protected Aminoethyl Quinoline Ligands in Palladium-Catalyzed β-C(sp3)–H Bond Arylation Reactions

Published:2019-09-29 Issue:42 Volume:141 Page:16726-16733
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Romero Erik A.¹^ORCID,Chen Gang²,Gembicky Milan¹,Jazzar Rodolphe¹^ORCID,Yu Jin-Quan²^ORCID,Bertrand Guy¹^ORCID

Affiliation:

1. UCSD-CNRS Joint Research Laboratory (UMI 3555), Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, California 92093-0358, United States

2. Department of Chemistry, The Scripps Research Institute, 10550 N. Torrey Pines Road, La Jolla, California 92037, United States

Funder

Division of Chemistry

Basic Energy Sciences

U.S. Department of Education

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.9b06746

Reference52 articles.