Organocatalytic Aryl–Aryl Bond Formation: An Atroposelective [3,3]-Rearrangement Approach to BINAM Derivatives-Reference-Cited by-同舟云学术

Organocatalytic Aryl–Aryl Bond Formation: An Atroposelective [3,3]-Rearrangement Approach to BINAM Derivatives

Published:2013-05-09 Issue:20 Volume:135 Page:7414-7417
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Li Gong-Qiang¹,Gao Hongyin¹,Keene Craig¹,Devonas Michael²,Ess Daniel H.²,Kürti László¹

Affiliation:

1. Division of Chemistry, Department of Biochemistry, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, Texas 75390, United States

2. Department of Chemistry and Biochemistry, Brigham Young University, Provo, Utah 84602, United States

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja401709k

Reference45 articles.

1. Atroposelective Synthesis of Axially Chiral Biaryl Compounds

2. bWolf, C.Dynamic Stereochemistry of Chiral Compounds: Principles and Applications;RSC:Cambridge, UK, 2007; Ch. 3, pp29–135.

3. Atroposelective Total Synthesis of Axially Chiral Biaryl Natural Products

4. Catalytic Asymmetric Synthesis

5. The Growing Impact of Catalysis in the Pharmaceutical Industry

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