Stereoselective synthesis of organosulfur compounds incorporating N-aromatic heterocyclic motifs and quaternary carbon centers via a sulfa-Michael triggered tandem reaction-Reference-Cited by-同舟云学术

Stereoselective synthesis of organosulfur compounds incorporating N-aromatic heterocyclic motifs and quaternary carbon centers via a sulfa-Michael triggered tandem reaction

Published:2015 Issue:47 Volume:51 Page:9714-9717
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Qin Tianyou¹²³⁴⁵,Cheng Lu⁵⁶⁷⁸⁴,Zhang Sean Xiao-An¹²³⁴⁵,Liao Weiwei⁵⁶⁷⁸⁴

Affiliation:

1. State Key Laboratory of Fine Chemicals

2. Dalian University of Technology

3. Dalian 116024

4. P. R. China

5. Department of Organic Chemistry

6. College of Chemistry

7. Jilin University

8. Changchun 130012

Abstract

The novel sulfa-Michael addition (SMA)-triggered tandem reaction was developed by combining a SMA reaction with a simultaneous rearomatization process.

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/C5CC01875G

Reference31 articles.

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3. Sulphur-Containing Drugs and Related Organic Compounds, ed. L. A. Damani, Wiley, New York, 1989

4. Asymmetric synthesis of tertiary thiols and thioethers

5. Organosulfur Chemistry in Asymmetric Synthesis, ed. T. Toru and C. Bolm, Wiley-VCH, Weinheim, Germany, 2008

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