Catalytic and Highly Efficient 1,4-Addition of Terminal Alkynes to Conjugated Enones by [RuCl2(p-cymene)]2/Pyrrolidine-Reference-Cited by-同舟云学术

Catalytic and Highly Efficient 1,4-Addition of Terminal Alkynes to Conjugated Enones by [RuCl2(p-cymene)]2/Pyrrolidine

Published:2001-06-01 Issue:13 Volume:3 Page:2089-2091
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Chang Sukbok¹,Na Youngim¹,Choi Eunjung¹,Kim Sunggak¹

Affiliation:

1. Department of Chemistry, Ewha Womans University, Seoul 120-750, Korea, and Center for Molecular Design and Synthesis, Department of Chemistry, Korea Advanced Institute of Science and Technology, Taejon 305-701, Korea

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol016047m

Reference20 articles.

1. Regio- and Stereochemical Aspects of the Palladium-Catalyzed Reactions of Silanes

2. Ruthenium-Catalyzed Reactions for Organic Synthesis

3. Element−Element Addition to Alkynes Catalyzed by the Group 10 Metals

4. General Synthesis of (Z)-Alk-1-en-1-yl Esters via Ruthenium-Catalyzed anti-Markovnikov trans-Addition of Carboxylic Acids to Terminal Alkynes

5. The First Example of Rhodium(I)-Catalyzed Regio- and Stereoselective Chloroesterification of Alkynes with Chloroformate Esters

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