In the last ten years organocatalysis has emerged as an efficient and sustainable strategy for the asymmetric synthesis of chiral molecules. Optically active intermediates for novel interesting transformations are generated under mild and operationally simple conditions when selenium-containing compounds are used as reaction partners. The peculiar reactivity of organoselenium compounds has been exploited in practical one-pot sequences for the asymmetric construction of densely functionalized compounds starting from simple precursors

Organocatalytic asymmetric synthesis and use of organoselenium compounds

Marini F.
;
Sternativo S.
2013

Abstract

In the last ten years organocatalysis has emerged as an efficient and sustainable strategy for the asymmetric synthesis of chiral molecules. Optically active intermediates for novel interesting transformations are generated under mild and operationally simple conditions when selenium-containing compounds are used as reaction partners. The peculiar reactivity of organoselenium compounds has been exploited in practical one-pot sequences for the asymmetric construction of densely functionalized compounds starting from simple precursors
2013
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11391/1542213
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