Piperazinylpyrimidine modified MCM-41 for the ecofriendly synthesis of benzothiazoles by the simple cleavage of disulfide in the presence of molecular O2-Reference-Cited by-同舟云学术

Piperazinylpyrimidine modified MCM-41 for the ecofriendly synthesis of benzothiazoles by the simple cleavage of disulfide in the presence of molecular O2

Published:2015 Issue:89 Volume:5 Page:72745-72754
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Ray Suman¹²³⁴,Das Paramita¹²³⁴,Banerjee Biplab⁵⁶⁷⁴,Bhaumik Asim⁵⁶⁷⁴,Mukhopadhyay Chhanda¹²³⁴

Affiliation:

1. Department of Chemistry

2. University of Calcutta

3. Kolkata -700009

4. India

5. Department of Materials Science

6. Indian Association for the Cultivation of Science

7. Kolkata 700 032

Abstract

Synthesis of benzothiazoles by metal free cleavage of disulfide bond.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA14894D

Reference102 articles.

1. 2-Arylbenzothiazole as a Privileged Scaffold in Drug Discovery

2. An efficient synthetic route to biologically relevant 2-phenylbenzothiazoles substituted on the benzothiazole ring

3. Synthesis and Evaluation of 11C-Labeled 6-Substituted 2-Arylbenzothiazoles as Amyloid Imaging Agents

4. Effects of Lipophilicity on the Affinity and Nonspecific Binding of Iodinated Benzothiazole Derivatives

5. A rapid one-step radiosynthesis of theβ-amyloid imaging radiotracerN-methyl-[11C]2-(4′-methylaminophenyl)-6-hydroxybenzothiazole([11C]-6-OH-BTA-1)

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