Ruthenium-Catalyzed Processes: Dual [2+2] Cycloaddition versus Cyclopropanation of Bicyclic Alkenes with Propargylic Alcohols-Reference-Cited by-同舟云学术

Ruthenium-Catalyzed Processes: Dual [2+2] Cycloaddition versus Cyclopropanation of Bicyclic Alkenes with Propargylic Alcohols

Published:2006-01-12 Issue:4 Volume:25 Page:843-848
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Villeneuve Karine¹,Tam William¹

Affiliation:

1. Guelph-Waterloo Centre for Graduate Work in Chemistry and Biochemistry, Department of Chemistry, University of Guelph, Guelph, Ontario, Canada N1G 2W1

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om050780q

Reference24 articles.

1. Ruthenium(II)-Catalyzed Cycloaddition of 1,6-Diynes with Isocyanates Leading to Bicyclic Pyridones

2. Ruthenium-Catalyzed Cycloaddition of 1,6-Diynes with Isothiocyanates and Carbon Disulfide: First Transition-Metal Catalyzed [2 + 2 + 2] Cocyclotrimerization Involving CS Double Bond

3. Ruthenium(II)-Catalyzed [2 + 2 + 2] Cycloaddition of 1,6-Diynes with Tricarbonyl Compounds

4. Propargyl Alcohols as Synthons for Allenols in Conjugate Addition

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