Iridium-catalyzed arylation of sulfoxonium ylides and arylboronic acids: a straightforward preparation of α-aryl ketones-Reference-Cited by-同舟云学术

Iridium-catalyzed arylation of sulfoxonium ylides and arylboronic acids: a straightforward preparation of α-aryl ketones

Published:2020 Issue:14 Volume:7 Page:1802-1808
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Shu Bing¹²³⁴⁵,Wang Xiao-Tong¹²³⁴⁵,Shen Zi-Xuan⁵²³⁶,Che Tong¹²³⁴,Zhong Mei⁵²³⁶,Song Jia-Lin⁵²³⁶,Kang Hua-Jie⁵²³⁶,Xie Hui¹²³⁴,Zhang Luyong¹²³⁴⁷,Zhang Shang-Shi¹²³⁴⁸^ORCID

Affiliation:

1. Center for Drug Research and Development

2. Guangdong Pharmaceutical University

3. Guangzhou

4. China

5. School of Pharmacy

6. PR China

7. Jiangsu Key Laboratory of Drug Screening

8. Guangzhou Key Laboratory of Construction and Application of New Drug Screening Model Systems

Abstract

A highly efficient iridium(iii)-catalyzed arylation coupling of sulfoxonium ylides with arylboronic acids to generate α-aryl ketones has been established for the first time.

Funder

Guangdong Pharmaceutical University

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/QO/D0QO00543F

Reference72 articles.

1. Exploration of Novel Aryl Binding Sites of Farnesyltransferase Using Molecular Modeling and Benzophenone-Based Farnesyltransferase Inhibitors

2. A Unique Catalyst Effects the Rapid Room-Temperature Cross-Coupling of Organozinc Reagents with Carboxylic Acid Fluorides, Chlorides, Anhydrides, and Thioesters

3. Synthesis of Trifluoromethylaryl Diazirine and Benzophenone Derivatives of Etomidate that Are Potent General Anesthetics and Effective Photolabels for Probing Sites on Ligand-Gated Ion Channels