Palladium/Azaphos-Catalyzed Asymmetric Suzuki–Miyaura Coupling-Reference-Cited by-同舟云学术

Palladium/Azaphos-Catalyzed Asymmetric Suzuki–Miyaura Coupling

Published:2023-04-05 Issue:16 Volume:55 Page:2537-2542
ISSN:0039-7881
Container-title:Synthesis
language:en
Short-container-title:Synthesis

Author:

Yang Zhiping¹,Wang Jun¹^ORCID,Jiang Yanxin¹,Cheng Kwai Wun¹,Zhang Haoyang²

Affiliation:

1. Department of Chemistry, Hong Kong Baptist University

2. Department of Chemistry, Southern University of Science and Technology

Abstract

AbstractA palladium-catalyzed asymmetric Suzuki–Miyaura coupling is described with a unique monophosphine ligand, Azaphos. This method provides a new ligand framework that could be used in asymmetric Suzuki–Miyaura coupling reactions to prepare the axially chiral compounds.

Funder

Research Grants Council of Hong Kong

Hong Kong Baptist University

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry,Catalysis

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/a-2069-4665.pdf

Reference50 articles.

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4. Transition-metal-catalyzed Suzuki–Miyaura cross-coupling reactions: a remarkable advance from palladium to nickel catalysts

5. Efficient Enantioselective Syntheses of Chiral Natural Products Facilitated by Ligand Design

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