Green Approaches To Asymmetric Catalytic Synthesis [recurso electrónico] / by Angela Patti.
Tipo de material: TextoSeries SpringerBriefs in Molecular Science ; 4Editor: Dordrecht : Springer Netherlands, 2011Descripción: XIV, 140p. 102 illus. online resourceTipo de contenido: text Tipo de medio: computer Tipo de portador: online resourceISBN: 9789400714540Tema(s): Chemistry | Environmental chemistry | Chemistry | Chemistry/Food Science, general | Environmental ChemistryFormatos físicos adicionales: Printed edition:: Sin títuloClasificación CDD: 540 Clasificación LoC:QD1-999Recursos en línea: Libro electrónicoTipo de ítem | Biblioteca actual | Colección | Signatura | Copia número | Estado | Fecha de vencimiento | Código de barras |
---|---|---|---|---|---|---|---|
Libro Electrónico | Biblioteca Electrónica | Colección de Libros Electrónicos | QD1 -999 (Browse shelf(Abre debajo)) | 1 | No para préstamo | 378515-2001 |
Methods for the preparation of optically active chiral compounds -- “Green” asymmetric synthesis: the catalysts -- Alternative solvents and recycle of the catalyst -- Technological tools and design of new chemical processes -- Technological tools and design of new chemical processes.
Nowadays, chirality is widely accepted as an important factor in molecular recognition processes and the biological activity of many pharmaceutical drugs and agrochemicals; this is confirmed by the continuous need for synthetic methods which lead to single or enriched enantiomers of such compounds. By presenting a review of the various and more recently developed approaches for both metal-transition and organocatalysis, this volume describes the development of “greener” asymmetric reactions which preserve stereoselectivity. The author summarizes the impressive amount of research that has been gathered within this field into three chapters focusing on: i)the search of alternative catalysts, ii) alternative solvents, and iii) alternative synthetic strategies and processes. For each topic, the fundamentals and some valuable applications are discussed.
19