Document Detail


Ruthenium-catalyzed ring-opening and ring-closing enyne metathesis.
MedLine Citation:
PMID:  11348184     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
[reaction: see text]. When a CH2Cl2 solution of an enyne containing the cycloalkene moiety was stirred in the presence of ruthenium-carbene complex (10 mol %) at room temperature under ethylene gas (1 atm), ring-opening and ring-closing metathesis occurred to afford cyclized triene. The reaction was carried out under argon gas, and no cyclized product was obtained. Enynes with a terminal alkyne gave good results.
Authors:
T Kitamura; M Mori
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Organic letters     Volume:  3     ISSN:  1523-7060     ISO Abbreviation:  Org. Lett.     Publication Date:  2001 Apr 
Date Detail:
Created Date:  2001-05-11     Completed Date:  2001-07-12     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  100890393     Medline TA:  Org Lett     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1161-3     Citation Subset:  IM    
Affiliation:
Graduate School of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan.
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MeSH Terms
Descriptor/Qualifier:
Alkenes / chemical synthesis*
Alkynes / chemical synthesis*
Argon / chemistry
Cycloparaffins / chemistry*
Models, Chemical
Ruthenium / chemistry*
Temperature
Time Factors
Chemical
Reg. No./Substance:
0/Alkenes; 0/Alkynes; 0/Cycloparaffins; 7440-18-8/Ruthenium; 7440-37-1/Argon

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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