Rare-Earth-Catalyzed Transsulfinamidation of Sulfinamides with Amines-Reference-Cited by-同舟云学术

Rare-Earth-Catalyzed Transsulfinamidation of Sulfinamides with Amines

Published:2021-04-21 Issue:9 Volume:23 Page:3718-3723
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wen Daheng¹,Zheng Qingshu¹,Wang Chaoyu¹,Tu Tao¹²³^ORCID

Affiliation:

1. Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Department of Chemistry, Fudan University, 2005 Songhu Road, Shanghai 200438, China

2. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China

3. Green Catalysis Center and College of Chemistry, Zhengzhou University, Zhengzhou 450001, China

Funder

Ministry of Science and Technology of the People's Republic of China

National Natural Science Foundation of China

Department of Chemistry, Fudan University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c01106

Reference45 articles.

1. A General Method for Two-Step Transamidation of Secondary Amides Using Commercially Available, Air- and Moisture-Stable Palladium/NHC (N-Heterocyclic Carbene) Complexes

2. Breaking Amides using Nickel Catalysis

3. An Efficient Heterobimetallic Lanthanide Alkoxide Catalyst for Transamidation of Amides under Solvent-Free Conditions

4. A two-step approach to achieve secondary amide transamidation enabled by nickel catalysis

5. Efficient Copper(II)-Catalyzed Transamidation of Non-Activated Primary Carboxamides and Ureas with Amines

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