P(NMe2)3-mediated reductive [1+4] annulation of isatins with enones: a facile synthesis of spirooxindole-dihydrofurans-Reference-Cited by-同舟云学术

P(NMe2)3-mediated reductive [1+4] annulation of isatins with enones: a facile synthesis of spirooxindole-dihydrofurans

Published:2015 Issue:78 Volume:51 Page:14663-14666
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Zhou Rong¹²³⁴,Zhang Kai¹²³⁴,Chen Yusong¹²³⁴,Meng Qiang¹²³⁴,Liu Yiyi⁵⁶⁷⁴,Li Ruifeng¹²³⁴,He Zhengjie⁵⁶⁷⁴⁸

Affiliation:

1. College of Chemistry and Chemical Engineering

2. Taiyuan University of Technology

3. Taiyuan

4. P. R. China

5. The State Key Laboratory of Elemento-Organic Chemistry

6. Nankai University

7. Tianjin

8. Collaborative Innovation Center of Chemical Science and Engineering

Abstract

A novel reductive [1+4] annulation reaction of isatins and enones via Kukhtin–Ramirez adducts is reported.

Funder

Natural Science Foundation of Shanxi Province

National Natural Science Foundation of China

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/2015/CC/C5CC03676C

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4. Recent Advances in Asymmetric Organocatalytic Construction of 3,3′-Spirocyclic Oxindoles

5. Organocatalytic Asymmetric Assembly Reactions: Synthesis of Spirooxindoles via Organocascade Strategies

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