Selective C–H chalcogenation of thiazoles via thiazol-2-yl-phosphonium salts-Reference-Cited by-同舟云学术

Selective C–H chalcogenation of thiazoles via thiazol-2-yl-phosphonium salts

Published:2020 Issue:27 Volume:18 Page:5183-5191
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Zi You¹²³⁴,Wagner Konrad¹²³⁴,Schömberg Fritz¹²³⁴,Vilotijevic Ivan¹²³⁴^ORCID

Affiliation:

1. Institute of Organic Chemistry and Macromolecular Chemistry

2. Friedrich Schiller University Jena

3. 07743 Jena

4. Germany

Abstract

Medicinally relevant substituted benzothiazoles and thiazoles are prepared under mild conditions by a regioselective C2–H chalcogenation via preparation of the phosphonium salt and the subsequent reaction with S- and Se-centered nucleophiles.

Funder

Carl-Zeiss-Stiftung

Friedrich-Schiller-Universität Jena

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/OB/D0OB00684J

Reference94 articles.

1. Benzobisthiazole-Based Semiconducting Copolymers Showing Excellent Environmental Stability in High-Humidity Air

2. Thiazole-Based Organic Semiconductors for Organic Electronics

3. Cruciform π-Systems for Molecular Electronics Applications

4. Rhodium-catalyzed synthesis of unsymmetrical di(aryl/heteroaryl)methanes using aryl/heteroarylmethyl ketones via CO–C bond cleavage

5. Rhodium-Catalyzed Synthesis of Unsymmetric Di(heteroaryl) Sulfides Using Heteroaryl Ethers and S-Heteroaryl Thioesters via Heteroarylthio Exchange

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