An Enantioselective Suzuki–Miyaura Coupling To Form Axially Chiral Biphenols-Reference-Cited by-同舟云学术

An Enantioselective Suzuki–Miyaura Coupling To Form Axially Chiral Biphenols

Published:2022-08-15 Issue:33 Volume:144 Page:15026-15032
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Pearce-Higgins Robert¹,Hogenhout Larissa N.¹,Docherty Philip J.¹,Whalley David M.¹,Chuentragool Padon¹^ORCID,Lee Najung¹,Lam Nelson Y. S.¹^ORCID,McGuire Thomas M.²,Valette Damien³^ORCID,Phipps Robert J.¹^ORCID

Affiliation:

1. Yusuf Hamied Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, United Kingdom

2. Oncology R&D, AstraZeneca, Cambridge CB4 0WG, United Kingdom

3. GlaxoSmithKline Medicines Research Centre, Stevenage, Hertfordshire SG1 2NY, United Kingdom

Funder

AstraZeneca

Engineering and Physical Sciences Research Council

Royal Society

GlaxoSmithKline

H2020 European Research Council

Trinity Hall College, University of Cambridge

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.2c06529

Reference70 articles.

1. Cross-Coupling Reactions Of Organoboranes: An Easy Way To Construct CC Bonds (Nobel Lecture)

2. The Challenge of Atropisomerism in Drug Discovery

3. Assessing Atropisomer Axial Chirality in Drug Discovery and Development

4. A twist of nature – the significance of atropisomers in biological systems

5. Atropisomerism in medicinal chemistry: challenges and opportunities

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