Regioselective enzymatic synthesis of estradiol 17-fatty acid esters

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A series of acyl esters of 3,17-β-estradiol has been prepared by an enzymatic methodology. Eleven 17-monoacyl products (five novel compounds) were obtained in a highly regioselective way by acylation of 3,17-β-estradiol or by alcoholysis of the corresponding diacyl derivatives. The influence of vari...

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Autores principales:	Rustoy, E.M., Ruiz Arias, I.E., Baldessari, A.
Formato:	Artículo publishedVersion
Publicado:	2005
Materias:	3,17-β-estradiol esters Enzymatic acylation and alcoholysis Lipases
Acceso en línea:	http://hdl.handle.net/20.500.12110/paper_14246376_v2005_n12_p175_Rustoy https://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_14246376_v2005_n12_p175_Rustoy_oai
Aporte de:	Repositorio Digital de la Universidad de Buenos Aires (UBA) de Universidad de Buenos Aires

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