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

By: Orru, Romano V. A [editor.].
Contributor(s): Ruijter, Eelco [editor.] | SpringerLink (Online service).
Material type: materialTypeLabelBookSeries: Topics in Heterocyclic Chemistry: 23Publisher: Berlin, Heidelberg : Springer Berlin Heidelberg : Imprint: Springer, 2010Description: XV, 280p. 87 illus. online resource.Content type: text Media type: computer Carrier type: online resourceISBN: 9783642126758.Subject(s): Chemistry | Biochemical engineering | Chemistry, Organic | Biochemistry | Chemistry | Organic Chemistry | Biochemical Engineering | Medicinal ChemistryDDC classification: 547 Online resources: Click here to access online
Contents:
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.
In: Springer eBooksSummary: 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: α-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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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: α-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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