@misc{10498/20594,
year = {2016},
url = {http://hdl.handle.net/10498/20594},
abstract = {A method has been developed for the conversion of primary, secondary, and tertiary alcohols, and phenol, into the
corresponding esters at room temperature. The method uses a titanium(III) species generated from a substoichiometric amount of titanocene dichloride together with manganese(0) as a reductant, as well as methylene diiodide. It involves a transesterification from an ethyl ester, or a reaction with an acyl chloride. A radical mechanism is proposed for these transformations.},
publisher = {Willey},
keywords = {Esters},
keywords = {Acylation},
keywords = {Radical reactions},
keywords = {Halohydrins},
keywords = {Titanium},
title = {Efficient O-Acylation of Alcohols and Phenol Using Cp2TiCl as a Reaction Promoter},
doi = {10.1002/ejoc.201600496},
author = {Durán Peña, María Jesús and Botubol Ares, José Manuel and R. Hanson, James and Hernández Galán, Rosario and González Collado, Isidro},
}