Ni-Catalyzed Suzuki–Miyaura Cross-Coupling of α-Oxo-vinylsulfones To Prepare C-Aryl Glycals and Acyclic Vinyl Ethers-Reference-Cited by-同舟云学术

Ni-Catalyzed Suzuki–Miyaura Cross-Coupling of α-Oxo-vinylsulfones To Prepare C-Aryl Glycals and Acyclic Vinyl Ethers

Published:2019-04-26 Issue:19 Volume:141 Page:7680-7686
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Gong Liang¹,Sun Hong-Bao¹,Deng Li-Fan¹,Zhang Xia¹,Liu Jie¹,Yang Shengyong¹^ORCID,Niu Dawen¹^ORCID

Affiliation:

1. Department of Emergency, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, and School of Chemical Engineering, Sichuan University, Chengdu 610041, China

Funder

Sichuan University

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.9b02312

Reference88 articles.

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

2. Analysis of Past and Present Synthetic Methodologies on Medicinal Chemistry: Where Have All the New Reactions Gone?

3. Development of a Concise Multikilogram Synthesis of LPA-1 Antagonist BMS-986020 via a Tandem Borylation–Suzuki Procedure

4. Evolution of a Strategy for Total Synthesis of the Marine Fungal Alkaloid (±)-Communesin F

5. Palladium-Catalyzed Regioselective Cross-Coupling Reactions of 3-Bromo-4-tosyloxyquinolin-2(1H)-one with Arylboronic Acids. A Facile and Convenient Route to 3,4-Disubstituted Quinolin-2(1H)-ones

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