| 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 |
