Issue 10, 1993

Stereoselective synthesis of Z-enol esters catalysed by [bis(diphenylphosphino)alkane]bis(2-methylpropenyl)ruthenium complexes

Abstract

Z-Enol esters are obtained via region- and stereo-selective addition of carboxylic acids to terminal alkynes, with formation of a C(1) carbon–oxygen bond, in the presence of a [Ru{Ph2P(CH2)nPPh2}{η3-CH2–C(Me)[double bond, length half m-dash]CH2}2] catalyst precursor.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1993, 850-851

Stereoselective synthesis of Z-enol esters catalysed by [bis(diphenylphosphino)alkane]bis(2-methylpropenyl)ruthenium complexes

H. Doucet, J. Höfer, C. Bruneau and P. H. Dixneuf, J. Chem. Soc., Chem. Commun., 1993, 850 DOI: 10.1039/C39930000850

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