Regioselective Alcoholysis and Hydrochlorination Reactions of Spiro-Epoxy Oxindoles at the Spiro-Centre: Synthesis of 3,3-Disubstituted Oxindoles and Application for Anticancer Agents-Reference-Cited by-同舟云学术

Regioselective Alcoholysis and Hydrochlorination Reactions of Spiro-Epoxy Oxindoles at the Spiro-Centre: Synthesis of 3,3-Disubstituted Oxindoles and Application for Anticancer Agents

Published:2018-10-24 Issue:41 Volume:2018 Page:5678-5687
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Tak Raj Kumar¹²^ORCID,Gupta Naveen¹²,Kumar Manish¹²,Kureshy Rukhsana I.¹²^ORCID,Khan Noor-ul H.¹²,Suresh E.²³

Affiliation:

1. Inorganic Materials and Catalysis Division; CSIR-Central Salt and Marine Chemicals Research Institute; G. B. Marg 364002, Gujarat Bhavnagar - India

2. Academy of Scientific and Innovative Research; CSIR-Central Salt and Marine Chemicals Research Institute; Council of Scientific & Industrial Research (CSIR); G. B. Marg 364002, Gujarat Bhavnagar - India

3. Analytical Division and Centralized Instrument Facility; CSIR-Central Salt and Marine Chemicals Research Institute; G. B. Marg 364002 Bhavnagar - Gujarat India

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201801002/fullpdf

Reference49 articles.

1. Therapeutic Potential of Spirooxindoles as Antiviral Agents

2. Recent Progress on Routes to Spirooxindole Systems Derived from Isatin

3. Paraherquamides, Brevianamides, and Asperparalines: Laboratory Synthesis and Biosynthesis. An Interim Report

4. Efficient synthesis of new 2,3-dihydrooxazole-spirooxindoles hybrids as antimicrobial agents

5. Spirooxindoles: Promising scaffolds for anticancer agents

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