Synthesis of Heterocycles via Multicomponent Reactions I
Synthesis of Heterocycles via Multicomponent Reactions I
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: -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
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.
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 HeterocyclizationsThe 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.
Orru, Romano V. A.
Ruijter, Eelco
ISBN | 978-3-642-12674-1 |
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Artikelnummer | 9783642126741 |
Medientyp | Buch |
Copyrightjahr | 2010 |
Verlag | Springer, Berlin |
Umfang | XV, 280 Seiten |
Abbildungen | XV, 280 p. 87 illus. |
Sprache | Englisch |