Copper promoted radical addition/cyclization of azobisisobutyronitrile with arylacrylamides: a convenient process to synthesize 3-(2′-cyano alkyl) oxindoles-Reference-Cited by-同舟云学术

Copper promoted radical addition/cyclization of azobisisobutyronitrile with arylacrylamides: a convenient process to synthesize 3-(2′-cyano alkyl) oxindoles

Published:2015 Issue:71 Volume:5 Page:57469-57471
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Wang Ruihong¹²³⁴,Bao Weiliang¹²³⁴

Affiliation:

1. Department of Chemistry

2. Zhejiang University (Xixi Campus)

3. Hangzhou 310028

4. People's Republic of China

Abstract

A CuI promoted radical addition/cyclization of azobisisobutyronitrile with alkenes for the preparation of 3-(2′-cyano alkyl) oxindoles was developed.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA07739G

Reference53 articles.

1. BMS-204352: A Potassium Channel Opener Developed for the Treatment of Stroke

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

5. Catalytic Asymmetric Synthesis of Oxindoles Bearing a Tetrasubstituted Stereocenter at the C-3 Position

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