Highly efficient endo’- selective synthesis of (dispiro 3,2′-pyrrolidinyl) bisoxindoles containing three contiguous chiral stereocenters with two contiguous quaternary spirostereocenters-Reference-Cited by-同舟云学术

Highly efficient endo’- selective synthesis of (dispiro 3,2′-pyrrolidinyl) bisoxindoles containing three contiguous chiral stereocenters with two contiguous quaternary spirostereocenters

Published:2020-06-20 Issue:1 Volume:132 Page:
ISSN:0974-3626
Container-title:Journal of Chemical Sciences
language:en
Short-container-title:J Chem Sci

Author:

Yuvaraj Panneerselvam^ORCID,Singh Huidrom Birkumar,Kandapalam Arun Prasath Lingam,Kathirvelan Devarajan,Nagarajan Sankaranarayanan

Funder

Science and Engineering Research Board

Publisher

Springer Science and Business Media LLC

Subject

General Chemistry

Link

https://link.springer.com/content/pdf/10.1007/s12039-020-01772-7.pdf

Reference39 articles.

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2. (b) Marti C and Carreira E M 2003 Construction of Spiro[pyrrolidine‐3,3′‐oxindoles] − Recent Applications to the Synthesis of Oxindole Alkaloids Eur. J. Org. Chem. 12 2209

3. (c) Trost B M and Brennan M K 2009 Asymmetric Syntheses of Oxindole and Indole Spirocyclic Alkaloid Natural Products Synthesis 18 3003

4. (a) Cui C B, Kakeya H and Osada H 1996 Novel mammalian cell cycle inhibitors, spirotryprostatins A and B, produced by Aspergillus fumigatus, which inhibit mammalian cell cycle at G2/M phase Tetrahedron 52 12651

5. (b) Cui C B, Kakeya H and Osada H 1996 Spirotryprostatin B, a novel mammalian cell cycle inhibitor produced by Aspergillus fumigatus J. Antibiot. 49 832

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