Gold-catalyzed formal [4π + 2π]-cycloadditions of propiolate derivatives with unactivated nitriles-Reference-Cited by-同舟云学术

Gold-catalyzed formal [4π + 2π]-cycloadditions of propiolate derivatives with unactivated nitriles

Published:2015 Issue:10 Volume:6 Page:5964-5968
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Karad Somnath Narayan¹²³⁴,Chung Wei-Kang¹²³⁴,Liu Rai-Shung¹²³⁴

Affiliation:

1. Department of Chemistry

2. National Tsing Hua University 101

3. Hsinchu

4. Taiwan

Abstract

Gold-catalyzed hetero-[4π + 2π]-cycloadditions of tert-butyl propiolates with unactivated nitriles are described. This new finding enables a one-pot gold-catalyzed synthesis of highly substituted pyridines.

Funder

National Science Council Taiwan

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/SC/C5SC01950H

Reference52 articles.

1. Transition Metal-Mediated Cycloaddition Reactions

2. Stereoselective transition metal-catalysed higher-order carbocyclisation reactions

3. Recent Developments in Catalytic Asymmetric Inverse-Electron-Demand Diels–Alder Reaction

4. Catalytic asymmetric Diels Alder reactions

5. Iron Catalysis in Organic Synthesis

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