Thiofunctionalization of Electron‐Rich Heteroarenes through Magnesiation and Trapping with Octasulfur-Reference-Cited by-同舟云学术

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Thiofunctionalization of Electron‐Rich Heteroarenes through Magnesiation and Trapping with Octasulfur

Published:2021-09-23 Issue:22 Volume:363 Page:5099-5105
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Vera Gonzalo¹,Mangeant Reynald¹,Stiebing Silvia¹,Berhault Yohann¹,Fabis Frédéric¹,Cailly Thomas¹²³⁴,Collot Valérie¹

Affiliation:

1. Normandie Univ UNICAEN Centre d'Etudes et de Recherche sur le Médicament de Normandie (CERMN) 14000 Caen France

2. Normandie Univ UNICAEN IMOGERE 14000 Caen France

3. CHU Côte de Nacre Department of Nuclear Medicine 14000 Caen France

4. Institut Blood and Brain@Caen-Normandie (BB@C) Boulevard Henri Becquerel 14074 Caen France

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.202100869

Reference42 articles.

1. Analysis of the Structural Diversity, Substitution Patterns, and Frequency of Nitrogen Heterocycles among U.S. FDA Approved Pharmaceuticals

2. Sulfur Containing Scaffolds in Drugs: Synthesis and Application in Medicinal Chemistry

3. The Medicinal Chemist’s Toolbox: An Analysis of Reactions Used in the Pursuit of Drug Candidates

4. Transition-Metal-Catalyzed C−S, C−Se, and C−Te Bond Formation via Cross-Coupling and Atom-Economic Addition Reactions

5. Recent developments in palladium-catalyzed C–S bond formation

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