Document Detail

Ru-catalyzed dehydrogenative coupling of carboxylic acids and silanes--a new method for the preparation of silyl ester.
MedLine Citation:
PMID:  18941497     Owner:  NLM     Status:  PubMed-not-MEDLINE    
Ru(3)(CO)(12)/EtI has been found to be an efficient catalyst system for the dehydrosilylation of carboxylic acids with silanes. In the presence of 1 mol% Ru(3)(CO)(12) and 4 mol% EtI, dehydrosilylation reactions in toluene afforded the corresponding silyl esters at 100 degrees C in good and high yields.
Guo-Bin Liu; Hong-Yun Zhao
Related Documents :
24134837 - A hydrophobic amino acid cluster inserted into the c-terminus of a recycling cell surfa...
24751157 - Design, synthesis and biological evaluation of peptidyl epoxyketone proteasome inhibito...
7119577 - Ionization behavior of aqueous short-chain carboxylic acids: a carbon-13 nmr study.
23316227 - In silico docking of hnf-1a receptor ligands.
2302867 - Comparative efficacy of dietary treatments on renal function in rats with sub-total nep...
20403687 - Xylose and cellulose fractionation from corncob with three different strategies and sep...
Publication Detail:
Type:  Journal Article     Date:  2008-07-30
Journal Detail:
Title:  Beilstein journal of organic chemistry     Volume:  4     ISSN:  1860-5397     ISO Abbreviation:  Beilstein J Org Chem     Publication Date:  2008  
Date Detail:
Created Date:  2008-10-22     Completed Date:  2010-05-20     Revised Date:  2013-05-23    
Medline Journal Info:
Nlm Unique ID:  101250746     Medline TA:  Beilstein J Org Chem     Country:  Germany    
Other Details:
Languages:  eng     Pagination:  27     Citation Subset:  -    
Department of Chemistry, Fudan University, 220 Handan Road, Shanghai 200433, P.R.China.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms

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

Previous Document:  Control of asymmetric biaryl conformations with terpenol moieties: syntheses, structures and energet...
Next Document:  Phase-vanishing halolactonization of neat substrates.