1,2-Amidoarylcarbonylation of Styrenes to Access β-Acylamino Ketones by NHC-Catalyzed Radical Relay-Reference-Cited by-同舟云学术

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1,2-Amidoarylcarbonylation of Styrenes to Access β-Acylamino Ketones by NHC-Catalyzed Radical Relay

Published:2024-08-28 Issue: Volume: Page:
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Yin Dengyu¹,Lu Lishuai¹,Jiang Ying¹,Dou Yandong²,Fu Ming-Chen¹^ORCID,Zhu Yanwu¹,Fan Shilu¹³^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering, Hefei University of Technology, Hefei 230009, China

2. Anhui Heryi Pharmaceutical Co., Ltd., Chuzhou 239000, China

3. Anhui Province Key Laboratory of Advance Catalytic Materials and Reaction Engineering, Hefei 230009, China

Funder

Fundamental Research Funds for the Central Universities

Anhui Provincial Key Research and Development Plan

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c01171

Reference38 articles.

1. I2-Catalyzed C–O Bond Formation and Dehydrogenation: Facile Synthesis of Oxazolines and Oxazoles Controlled by Bases

2. Metal-free annulation of β-acylamino ketones: facile access to spirooxazolines and oxazolines via oxidative C–O bond formation

3. Iodine-Mediated Oxidative Dehydrogenation of β-Acylamino Ketones for the Highly Stereoselective Synthesis of (Z)-β-Ketoenamides

4. Highly Enantioselective Hydrogenation of β-Ketoenamides with the Rh-ZhangPhos Catalyst

5. Rhodium-Catalyzed Enantioselective and Diastereoselective Hydrogenation of β-Ketoenamides: Efficient Access toanti1,3-Amino Alcohols

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