First Desymmetrization of 1,3-Propanediamine Derivatives in Organic Solvent. Development of a New Route for the Preparation of Optically Active Amines§

dc.contributor.author	Busto García, Benjamín Eduardo
dc.contributor.author	Gotor Fernández, Vicente
dc.contributor.author	García-Granda, Santiago
dc.contributor.author	Gotor Santamaría, Vicente Miguel
dc.date.accessioned	2020-05-20T09:21:55Z
dc.date.available	2020-05-20T09:21:55Z
dc.date.issued	2007
dc.identifier.citation	Organic Letters, 9(21), p. 4203–4206 (2007); doi:10.1021/ol701720m
dc.identifier.issn	1523-7060
dc.identifier.uri	http://hdl.handle.net/10651/54887
dc.description.abstract	The chemical synthesis and enzymatic desymmetrization of a panel of prochiral diamines have been successfully described for the first time using lipases in organic solvents. A family of 2-aryl-1,3-propanediamines has been obtained with high enantiopurity and good yields in the PSL-catalyzed reaction using diallyl carbonate in 1,4-dioxane.	spa
dc.format.extent	p. 4203–4206	spa
dc.language.iso	eng	spa
dc.relation.ispartof	Organic Letters, 9	spa
dc.rights	© 2007 American Chemical Society
dc.title	First Desymmetrization of 1,3-Propanediamine Derivatives in Organic Solvent. Development of a New Route for the Preparation of Optically Active Amines§	spa
dc.type	journal article	spa
dc.identifier.doi	10.1021/ol701720m
dc.relation.publisherversion	https://doi.org/10.1021/ol701720m	spa

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