Ruthenium-Catalyzed Cyclization of Epoxide with a Tethered Alkyne: Formation of Ketene Intermediates via Oxygen Transfer from Epoxides to Terminal Alkynes-Reference-Cited by-同舟云学术

Ruthenium-Catalyzed Cyclization of Epoxide with a Tethered Alkyne: Formation of Ketene Intermediates via Oxygen Transfer from Epoxides to Terminal Alkynes

Published:2004-05-14 Issue:22 Volume:126 Page:6895-6899
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Madhushaw Reniguntala J.¹,Lin Ming-Yuan¹,Sohel Shariar Md. Abu¹,Liu Rai-Shung¹

Affiliation:

1. Contribution from the Department of Chemistry, National Tsing-Hua University, Hsinchu, Taiwan, Republic of China

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja049943c

Reference25 articles.

1. A Short Synthesis of the Potent Antitumor Agent (±)-Hydroxymethylacylfulvene Using an Allenic Pauson-Khand Type Cycloaddition

2. Selective Generation of Free Radicals from Epoxides Using a Transition-Metal Radical. A Powerful New Tool for Organic Synthesis

3. Catalytic, Highly Regio- and Chemoselective Generation of Radicals from Epoxides: Titanocene Dichloride as an Electron Transfer Catalyst in Transition Metal Catalyzed Radical Reactions

4. A New Co2(CO)8-Mediated Tandem [5 + 1]/[2 + 2 + 1]-Cycloaddition Reaction: A One-Pot Synthesis of Tricyclic δ-Lactones from cis-Epoxy Ene-ynes

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