Journal
CHEMICAL COMMUNICATIONS
Volume 49, Issue 7, Pages 710-712Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c2cc38454j
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Funding
- Hong Kong Polytechnic University
- Innovation and Technology Commission
- Research Grants Council [PolyU 5015/07P]
- University Grants Committee [SEG_PolyU01]
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A dinuclear ruthenium catalyst with a rigid anthracene spacer shows excellent regio- and stereo-selectivity in the atom-economic addition of aliphatic carboxylic acids to phenylacetylene, producing exclusively anti-Markovnikov enol-esters with high E/Z ratios of the isomers.
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