Aminophosphonite-phosphite and aminophosphonite-phosphinite chiral ligands with mixed stereogenic elements have been prepared in good yields from chiral α-aminoalcohols such as 2-(hydroxymethyl)pyrrolidine and 2-N-ethylammino-1-butanol. These new ligands have been fully characterized; the Rh(I) complexes have been tested in catalytic hydrogenation and hydroformylation reactions. Enantioselectivities up to 70% have been obtained in asymmetric hydrogenation of α-acetamidocinnamic acid, methyl ester; enantioselectivities higher than 30% and regioselectivities higher than 98% have been obtained in asymmetric hydroformylation of vinyl acetate.
Aminophosphonite-phosphite and aminophosphonite-phosphinite ligands with mixed chirality: preparation and catalytic applications in asymmetric hydrogenation and hydroformylation / E. Cesarotti, S.Araneo, I. Rimoldi, S. Tassi. - In: JOURNAL OF MOLECULAR CATALYSIS. A: CHEMICAL. - ISSN 1381-1169. - 204-205(2003), pp. 211-220.
Aminophosphonite-phosphite and aminophosphonite-phosphinite ligands with mixed chirality: preparation and catalytic applications in asymmetric hydrogenation and hydroformylation
E. CesarottiPrimo
;S.AraneoSecondo
;I. RimoldiPenultimo
;
2003
Abstract
Aminophosphonite-phosphite and aminophosphonite-phosphinite chiral ligands with mixed stereogenic elements have been prepared in good yields from chiral α-aminoalcohols such as 2-(hydroxymethyl)pyrrolidine and 2-N-ethylammino-1-butanol. These new ligands have been fully characterized; the Rh(I) complexes have been tested in catalytic hydrogenation and hydroformylation reactions. Enantioselectivities up to 70% have been obtained in asymmetric hydrogenation of α-acetamidocinnamic acid, methyl ester; enantioselectivities higher than 30% and regioselectivities higher than 98% have been obtained in asymmetric hydroformylation of vinyl acetate.Pubblicazioni consigliate
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