Synthesis of Heterocycles via Multicomponent Reactions I (Topics in Heterocyclic Chemistry, 23)

✍ Scribed by Romano V. A. Orru (editor), Eelco Ruijter (editor)

• Publisher: Springer
• Year: 2010
• Tongue: English
• Leaves: 292
• Category: Library

✦ Synopsis

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

✦ Table of Contents

Synthesis of Heterocycles via Multicomponent Reactions I
Topics in Heterocyclic Chemistry Also Available Electronically
Aims and Scope
Preface
Contents
Synthesis of Heterocycles Through Classical Ugi and Passerini Reactions Followed by Secondary Transformations Involving One or
Aminoazoles as Key Reagents in Multicomponent Heterocyclizations
The Piperazine Space in Isocyanide-based MCR Chemistry
α-Acidic Isocyanides in Multicomponent Chemistry
Microreactor Technology as an Efficient Tool for Multicomponent Reactions
Cyclic Peptidomimetics and Pseudopeptides from Multicomponent Reactions
beta-Diketo Building Blocks for MCRs-Based Syntheses of Heterocycles
Index