Vinylogous Michael addition of nitroalkylideneoxindoles to isatylidene-malononitriles in the regio- and diastereoselective synthesis of dispirocyclopentylbisoxindoles-Reference-Cited by-同舟云学术

Vinylogous Michael addition of nitroalkylideneoxindoles to isatylidene-malononitriles in the regio- and diastereoselective synthesis of dispirocyclopentylbisoxindoles

Published:2023-01-02 Issue:1 Volume:135 Page:
ISSN:0973-7103
Container-title:Journal of Chemical Sciences
language:en
Short-container-title:J Chem Sci

Author:

Satham Lakshminarayana,Sankara Chenikkayala Siva,Bhagat Shweta,Namboothiri Irishi N N^ORCID

Funder

Science and Engineering Research Board, India

Publisher

Springer Science and Business Media LLC

Subject

General Chemistry

Link

https://link.springer.com/content/pdf/10.1007/s12039-022-02122-5.pdf

Reference68 articles.

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2. (b) Ye N, Chen E A, Wold E A, Shi P Y and Zhou J 2016 Therapeutic Potential of Spirooxindoles as Antiviral Agents ACS Infect. Dis. 2 382

3. (c) Yu B, Yu D Q and Liu H M 2015 Spirooxindoles: Promising Scaffolds for Anticancer Agents Eur. J. Med. Chem. 97 673

4. (d) Zheng Y, Tice C M and Singh S B 2014 The Use of Spirocyclic Scaffolds in Drug Discovery Bioorg. Med. Chem. Lett. 24 3673

5. (e) Galliford C V and Scheidt K A 2007 Pyrrolidinyl-Spirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents Angew. Chem., Int. Ed. 46 8748

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1. Regio- and diastereoselective synthesis of thioxothiazolidin-indolin-2-ones, oxoindolin-carbamodithioate hybrids, and their base-catalyzed conversion into dispirocyclopentanebisoxindoles;Scientific Reports;2024-06-20

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