Selective C3-Allylation and Formal [3 + 2]-Annulation of Spiro-Aziridine Oxindoles: Synthesis of 5′-Substituted Spiro[pyrrolidine-3,3′-oxindoles] and Coerulescine-Reference-Cited by-同舟云学术

Selective C3-Allylation and Formal [3 + 2]-Annulation of Spiro-Aziridine Oxindoles: Synthesis of 5′-Substituted Spiro[pyrrolidine-3,3′-oxindoles] and Coerulescine

Published:2022-06-22 Issue:13 Volume:87 Page:8656-8671
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Saleh SK Abu¹²,Hazra Atanu¹²^ORCID,Singh Maya Shankar²^ORCID,Hajra Saumen¹^ORCID

Affiliation:

1. Centre of Biomedical Research, Sanjay Gandhi Post-Graduate Institute of Medical Sciences Campus, Raebareli Road, Lucknow 226014, India

2. Department of Chemistry, Institute of Science, Banaras Hindu University, Varanasi 221005, India

Funder

Council of Scientific and Industrial Research

University Grants Commission

Science and Engineering Research Board

Centre of Bio-Medical Research

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c00863

Reference86 articles.

1. Novel mammalian cell cycle inhibitors, spirotryprostatins A and B, produced by Aspergillus fumigatus, which inhibit mammalian cell cycle at G2/M phase

2. Construction of Spiro[pyrrolidine‐3,3′‐oxindoles] − Recent Applications to the Synthesis of Oxindole Alkaloids

3. Pyrrolidinyl-Spirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents

4. Asymmetric Syntheses of Oxindole and Indole Spirocyclic Alkaloid Natural Products

5. Synthesis of Natural Product Inspired Compound Collections

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