Nickel-Catalyzed Reductive Cross-Coupling of N-Acyl and N-Sulfonyl Benzotriazoles with Diverse Nitro Compounds: Rapid Access to Amides and Sulfonamides-Reference-Cited by-同舟云学术

Nickel-Catalyzed Reductive Cross-Coupling of N-Acyl and N-Sulfonyl Benzotriazoles with Diverse Nitro Compounds: Rapid Access to Amides and Sulfonamides

Published:2021-12-14 Issue:1 Volume:24 Page:58-63
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Qu Erdong¹,Li Shangzhang¹,Bai Jin¹,Zheng Yan¹,Li Wanfang¹^ORCID

Affiliation:

1. School of Materials and Chemistry, University of Shanghai for Science and Technology, Shanghai 200093, P. R. China

Funder

Shanghai Municipal Education Commission

National Natural Science Foundation of China

Shanghai Engineering Research Center for Food Rapid Detection

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c03535

Reference47 articles.

1. Handbook of Bond Dissociation Energies in Organic Compounds

2. Conquering amide planarity: Structural distortion and its hidden reactivity

3. Mild, Metal-Free and Protection-Free Transamidation of N-Acyl-2-piperidones to Amino Acids, Amino Alcohols and Aliphatic Amines and Esterification of N-Acyl-2-piperidones

4. One-pot transition-metal free transamidation to sterically hindered amides

5. Ring Opening/Site Selective Cleavage in N-Acyl Glutarimide to Synthesize Primary Amides

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