Synthesis of Heterocycles via Multicomponent Reactions I [recurso electrónico] / edited by Romano V. A. Orru, Eelco Ruijter.

Por: Orru, Romano V. A [editor.]Colaborador(es): Ruijter, Eelco [editor.] | SpringerLink (Online service)Tipo de material: TextoTextoSeries Topics in Heterocyclic Chemistry ; 23Editor: Berlin, Heidelberg : Springer Berlin Heidelberg : Imprint: Springer, 2010Descripción: XV, 280p. 87 illus. online resourceTipo de contenido: text Tipo de medio: computer Tipo de portador: online resourceISBN: 9783642126758Tema(s): Chemistry | Biochemical engineering | Chemistry, Organic | Biochemistry | Chemistry | Organic Chemistry | Biochemical Engineering | Medicinal ChemistryFormatos físicos adicionales: Printed edition:: Sin títuloClasificación CDD: 547 Clasificación LoC:QD415-436Recursos en línea: Libro electrónicoTexto
Contenidos:
Synthesis of Heterocycles Through Classical Ugi and Passerini Reactions Followed by Secondary Transformations Involving One or Two Additional Functional Groups -- Aminoazoles as Key Reagents in Multicomponent Heterocyclizations -- The Piperazine Space in Isocyanide-based MCR Chemistry -- ?-Acidic Isocyanides in Multicomponent Chemistry -- Microreactor Technology as an Efficient Tool for Multicomponent Reactions -- Cyclic Peptidomimetics and Pseudopeptides from Multicomponent Reactions -- ?-Diketo Building Blocks for MCRs-Based Syntheses of Heterocycles.
En: Springer eBooksResumen: Contents: L. Banfi · A. Basso · R. Riva: Synthesis of Heterocycles Through Classical Ugi and Passerini Reactions Followed by Secondary Transformations Involving One or Two Additional Functional Groups.- V.A. Chebanov · K. A. Gura · S.M. Desenko: Aminoazoles as Key Reagents in Multicomponent Heterocyclizations.- Y. Huang · K. Khoury · A. Dömling: Piperazine Scaffolds by Multicomponent 3 Reactions: The Piperazine Space 4 in MCR Chemistry 5 Deep MCR Piperazine Space.- N. Elders · E. Ruijter · V.G. Nenajdenko · R.V.A. Orru: a-Acidic Isocyanides in Multicomponent Chemistry.- A. Cukalovic · J.-C.M.R. Monbaliu · C.V. Stevens: Microreactor Technology as an Efficient Tool for Multicomponent Reactions.- L.A. Wessjohann · C.R.B. Rhoden · D.G. Rivera · O. Eichler Vercillo: Cyclic Peptidomimetics and Pseudopeptides from Multicomponent Reactions.- M. del Mar Sanchez Duque · C. Allais · N. Isambert · T. Constantieux · J. Rodriguez: ß-Diketo Building Blocks for MCRs-Based Syntheses of Heterocycles
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Libro Electrónico Biblioteca Electrónica
Colección de Libros Electrónicos QD415 -436 (Browse shelf(Abre debajo)) 1 No para préstamo 374323-2001

Synthesis of Heterocycles Through Classical Ugi and Passerini Reactions Followed by Secondary Transformations Involving One or Two Additional Functional Groups -- Aminoazoles as Key Reagents in Multicomponent Heterocyclizations -- The Piperazine Space in Isocyanide-based MCR Chemistry -- ?-Acidic Isocyanides in Multicomponent Chemistry -- Microreactor Technology as an Efficient Tool for Multicomponent Reactions -- Cyclic Peptidomimetics and Pseudopeptides from Multicomponent Reactions -- ?-Diketo Building Blocks for MCRs-Based Syntheses of Heterocycles.

Contents: L. Banfi · A. Basso · R. Riva: Synthesis of Heterocycles Through Classical Ugi and Passerini Reactions Followed by Secondary Transformations Involving One or Two Additional Functional Groups.- V.A. Chebanov · K. A. Gura · S.M. Desenko: Aminoazoles as Key Reagents in Multicomponent Heterocyclizations.- Y. Huang · K. Khoury · A. Dömling: Piperazine Scaffolds by Multicomponent 3 Reactions: The Piperazine Space 4 in MCR Chemistry 5 Deep MCR Piperazine Space.- N. Elders · E. Ruijter · V.G. Nenajdenko · R.V.A. Orru: a-Acidic Isocyanides in Multicomponent Chemistry.- A. Cukalovic · J.-C.M.R. Monbaliu · C.V. Stevens: Microreactor Technology as an Efficient Tool for Multicomponent Reactions.- L.A. Wessjohann · C.R.B. Rhoden · D.G. Rivera · O. Eichler Vercillo: Cyclic Peptidomimetics and Pseudopeptides from Multicomponent Reactions.- M. del Mar Sanchez Duque · C. Allais · N. Isambert · T. Constantieux · J. Rodriguez: ß-Diketo Building Blocks for MCRs-Based Syntheses of Heterocycles

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