TBATB mediated debenzylative cross-coupling of aryl benzyl sulfides with electron rich compounds: synthesis of diaryl sulfides-Reference-Cited by-同舟云学术

TBATB mediated debenzylative cross-coupling of aryl benzyl sulfides with electron rich compounds: synthesis of diaryl sulfides

Published:2015 Issue:33 Volume:5 Page:25765-25767
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Hazarika Sukanya¹²³,Gogoi Prasanta¹²³,Barman Pranjit¹²³

Affiliation:

1. Department of Chemistry

2. National Institute of Technology

3. India

Abstract

An efficient TBATB mediated debenzylative cross coupling of aryl benzyl sulfides with electron rich compounds provides diaryl sulfides in moderate to excellent yield.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA00677E

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1. Trypanothione reductase inhibition/trypanocidal activity relationships in a 1,4-bis(3-aminopropyl)piperazine series

2. Discovery of Novel p-Arylthio Cinnamides as Antagonists of Leukocyte Function-Associated Antigen-1/Intracellular Adhesion Molecule-1 Interaction. 1. Identification of an Additional Binding Pocket Based on an Anilino Diaryl Sulfide Lead

3. Copper-Mediated Cross-Coupling of Aryl Boronic Acids and Alkyl Thiols

4. Organocatalytic Carbon–Sulfur Bond-Forming Reactions

5. A Mild, Nonbasic Synthesis of Thioethers. The Copper-Catalyzed Coupling of Boronic Acids with N-Thio(alkyl, aryl, heteroaryl)imides

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