Iron/copper co-catalyzed highly selective arylation of sulfinamides with aryl iodides-Reference-Cited by-同舟云学术

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Iron/copper co-catalyzed highly selective arylation of sulfinamides with aryl iodides

Published:2019-10 Issue:43 Volume:60 Page:151167
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Qin Shuanglin,Luo Yunhao,Sun Yue,Tian Le,Jiang Shende,yan Jun,Yang Guang^ORCID

Funder

National Natural Science Foundation of China

China National Major Scientific and Technological Special Project for “Significant New Drugs Development”

Tianjin Science and Technology Project

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference50 articles.

1. Synthesis and Applications of tert-Butanesulfinamide

2. Catalytic Asymmetric Synthesis of tert-Butanesulfinamide. Application to the Asymmetric Synthesis of Amines

3. Formal Synthesis of (−)-Aphanorphine Using Sequential Photomediated Radical Reactions of Dithiocarbamates

4. Asymmetric Copper-Catalyzed Synthesis of α-Amino Boronate Esters from N-tert-Butanesulfinyl Aldimines

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1. Ligand‐Promoted Catalysed Reactions;Organic Reaction Mechanisms Series;2023-01-20

2. Nickel-Catalyzed N-Arylation of Sulfinamides: A Comparative Study versus Analogous Sulfonamide Cross-Couplings;Organometallics;2022-12-27

3. An Optimized Ni‐catalyzed Chan‐Lam Type Coupling: Enantioretentive Access to Chiral N‐Aryl Sulfinamides;Chemistry – A European Journal;2022-10-25

4. Iron–Copper Dual Catalysis Enabling C−C and C−X (X=N, B, P, S, Sn) Bond Formation;European Journal of Organic Chemistry;2022-08-08

5. An Efficient Method for the Preparation of Sulfonamides from Sodium Sulfinates and Amines;ChemistryOpen;2022-08

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