Catalytic enantioselective synthesis of tetrasubstituted chromanones via palladium-catalyzed asymmetric conjugate arylation using chiral pyridine-dihydroisoquinoline ligands-Reference-Cited by-同舟云学术

Catalytic enantioselective synthesis of tetrasubstituted chromanones via palladium-catalyzed asymmetric conjugate arylation using chiral pyridine-dihydroisoquinoline ligands

Published:2020 Issue:18 Volume:11 Page:4602-4607
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Baek Doohyun¹²³⁴^ORCID,Ryu Huijeong¹²³⁴^ORCID,Ryu Ji Yeon¹⁵⁶⁴,Lee Junseong¹⁵⁶⁴^ORCID,Stoltz Brian M.⁷⁸⁹¹⁰¹¹^ORCID,Hong Sukwon¹²³⁴¹²^ORCID

Affiliation:

1. Department of Chemistry

2. Gwangju Institute of Science and Technology

3. Gwangju 61005

4. Republic of Korea

5. Chonnam National University

6. Gwangju 61186

7. The Warren and Katharine Schlinger Laboratory of Chemistry and Chemical Engineering

8. Division of Chemistry and Chemical Engineering

9. California Institute of Technology

10. Pasadena

11. USA

12. School of Materials Science and Engineering

Abstract

The first palladium-catalyzed enantioselective conjugate addition reactions of arylboronic acids to 2-substituted chromones with chiral pyridine-dihydroisoquinoline ligands have been developed.

Funder

National Institute of General Medical Sciences

National Research Foundation of Korea

Gwangju Institute of Science and Technology

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/SC/D0SC00412J

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