Copper-catalyzed alkylarylation of activated alkenes using isocyanides as the alkyl source: an efficient radical access to 3,3-dialkylated oxindoles-Reference-Cited by-同舟云学术

Copper-catalyzed alkylarylation of activated alkenes using isocyanides as the alkyl source: an efficient radical access to 3,3-dialkylated oxindoles

Published:2016 Issue:38 Volume:52 Page:6395-6398
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Zhao Yaping¹²³⁴⁵,Li Zhenghua¹²³⁴⁵,Sharma Upendra K.¹²³⁴⁵,Sharma Nandini¹²³⁴⁵,Song Gonghua⁶⁷⁸⁹,Van der Eycken Erik V.¹²³⁴⁵

Affiliation:

1. Laboratory for Organic & Microwave-Assisted Chemistry (LOMAC)

2. Department of Chemistry

3. University of Leuven (KU Leuven)

4. B-3001 Leuven

5. Belgium

6. Shanghai Key Laboratory of Chemical Biology

7. East China University of Science and Technology

8. Shanghai 200237

9. People's Republic of China

Abstract

A novel copper-catalyzed oxidative cyclization of N-arylacrylamides for the synthesis of 3,3-dialkylated oxindoles is described using isocyanides as alkyl radical precursors.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2016/CC/C6CC02024K

Reference72 articles.

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2. Recent advances in organocatalytic methods for the synthesis of disubstituted 2- and 3-indolinones

3. Transition‐Metal‐Mediated Routes to 3,3‐Disubstituted Oxindoles through Anilide Cyclisation

4. Formation of five- and six-membered heterocyclic rings under radical cyclisation conditions

5. Visible Light Photocatalysis: The Development of Photocatalytic Radical Ion Cycloadditions

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