Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.jorganchem.2005.11.023
Title: Regio- and stereoselective addition of carboxylic acids to phenylacetylene catalyzed by cyclopentadienyl ruthenium complexes
Authors: Ye, S.
Leong, W.K. 
Keywords: Anti-Markovnikov
Carboxylic acid
Enol esters
Phenylacetylene
Ruthenium
Issue Date: 1-Mar-2006
Citation: Ye, S., Leong, W.K. (2006-03-01). Regio- and stereoselective addition of carboxylic acids to phenylacetylene catalyzed by cyclopentadienyl ruthenium complexes. Journal of Organometallic Chemistry 691 (6) : 1117-1120. ScholarBank@NUS Repository. https://doi.org/10.1016/j.jorganchem.2005.11.023
Abstract: The direct addition of carboxylic acids to terminal alkynes such as phenylacetylene in the presence of catalytic amount of [CpRu(CO)2Cl] (1) or [{CpRu(CO)2}2] (2) affords the anti-Markovnikov adducts with high selectivity. In most instances, the E-enol esters are the major products. © 2005 Elsevier B.V. All rights reserved.
Source Title: Journal of Organometallic Chemistry
URI: http://scholarbank.nus.edu.sg/handle/10635/94709
ISSN: 0022328X
DOI: 10.1016/j.jorganchem.2005.11.023
Appears in Collections:Staff Publications

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