A Conformational Model for MTPA Esters of Chiral N-(2-Hydroxyalkyl)acrylamides

Rustoy, Eduardo Miguel; Baldessari, Alicia; Monsalve, Leandro Nicolas

info:eu-repo/semantics/article

Fecha

2014-05

Registro en:

Rustoy, Eduardo Miguel; Baldessari, Alicia; Monsalve, Leandro Nicolas; A Conformational Model for MTPA Esters of Chiral N-(2-Hydroxyalkyl)acrylamides; Hindawi Publishing Corporation; Advances in Chemistry; 2014; 7364; 5-2014; 1-6

2356-6612

http://hdl.handle.net/11336/18704

2314-7571

CONICET Digital

CONICET

Autor

Rustoy, Eduardo Miguel

Baldessari, Alicia

Monsalve, Leandro Nicolas

Institución

Consejo Nacional de Investigaciones Científicas y Tecnológicas (Argentina)

Resumen

The absolute stereochemistry of novel chiral N-(2-hycroxyalkyl)acrylamides prepared by a lipase-catalyzed resolution was successfully determined by 1H NMR of their MTPA esters. The method was validated for this particular case by computational experiments.

Materias

ABSOLUTE STEREOCHEMISTRY

CHIRAL

ACRYLAMIDES

LIPASE-CATALYZED

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