A Regioselective Synthesis of Carbazole‐Appended Dispiropyrrolothiazoles/Pyrrolidines: Synthesis, Computational Studies and In Vitro Anticancer Activity-Reference-Cited by-同舟云学术

A Regioselective Synthesis of Carbazole‐Appended Dispiropyrrolothiazoles/Pyrrolidines: Synthesis, Computational Studies and In Vitro Anticancer Activity

Published:2019-09-02 Issue:33 Volume:4 Page:9540-9549
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Arya Kripalaya Ratheesh¹,Sparkes Hazel A.²,Pandiyan Baskaran Vijaya³,Rajendra Prasad Karnam Jayarampillai¹^ORCID

Affiliation:

1. Department of ChemistryBharathiar University Coimbatore - 641046 India

2. School of ChemistryUniversity of Bristol, Cantock's Close, Bristol, BS8 1TS United Kingdom

3. Department of PhysicsBharathiar University Coimbatore - 641046 India

Funder

UGC-Emeritus fellowship

University Grant Commission

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.201801331

Reference53 articles.

1. A regio- and stereoselective 1,3-dipolar cycloaddition for the synthesis of new-fangled dispiropyrrolothiazoles as antimycobacterial agents

2. Asymmetric construction of 3-vinylidene-pyrrolidine derivatives containing allene moiety via Ag(i)/TF-BiphamPhos-catalyzed 1,3-dipolar cycloaddition of azomethine ylides with diethyl 2-(3,3-diphenylpropa-1,2-dienylidene) malonate

3. A facile regio- and stereoselective synthesis of novel dispirooxindolyl-[acridine-2′,3-pyrrolidine/thiapyrrolizidine]-1′-ones via 1,3-dipolar cycloaddition of azomethine ylides

4. Novel diastereoselective synthesis of spiropyrrolidine-oxindole derivatives as anti-breast cancer agents

5. Synthesis and Pharmacological Activities of Novel Bicyclic Thiazoline Derivatives as Hepatoprotective Agents. II. (7-Alkoxycarbonyl-2,3,5,6-tetrahydropyrrolo(2,1-b)thiazol-3-ylidene)acetamide Derivatives.

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1. Nitrone and Alkyne Cascade Reactions for Regio‐ and Diastereoselective 1‐Pyrroline Synthesis;Angewandte Chemie International Edition;2021-04-28

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