A facile and efficient synthesis of 3-spirocyclopentene-2-oxindoles via palladium mediated vinylcyclopropane–cyclopentene rearrangement of oxindole derived vinylcyclopropanes-Reference-Cited by-同舟云学术

A facile and efficient synthesis of 3-spirocyclopentene-2-oxindoles via palladium mediated vinylcyclopropane–cyclopentene rearrangement of oxindole derived vinylcyclopropanes

Published:2013-08 Issue:32 Volume:54 Page:4202-4206
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Lingam Kandapalam Arun Prasath,Shanmugam Ponnusamy

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference39 articles.

1. Construction of bispirooxindoles containing three quaternary stereocentres in a cascade using a single multifunctional organocatalyst

2. Biosynthetic Studies of the Notoamides: Isotopic Synthesis of Stephacidin A and Incorporation into Notoamide B and Sclerotiamide

3. Highly enantioselective synthesis and cellular evaluation of spirooxindoles inspired by natural products

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

5. Asymmetic Organocatalytic 1,3-Dipolar Cycloaddition of Azomethine Ylide to Methyl 2-(2-Nitrophenyl)acrylate for the Synthesis of Diastereoisomers of Spirotryprostatin A

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2. Ni(NHC) Catalyzed Rearrangement of 1‐Acyl‐2‐vinylcyclopropanes: Tackling a Mechanistic Puzzle by Combined Experimental and Computational Studies;European Journal of Organic Chemistry;2019-09-04

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