Synthesis of Heterocycles via Multicomponent Reactions I
(Sprache: Englisch)
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...
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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
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. D?ng: 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: ?Diketo Building Blocks for MCRs-Based Syntheses of Heterocycles
- 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. D?ng: 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: ?Diketo Building Blocks for MCRs-Based Syntheses of Heterocycles
Inhaltsverzeichnis zu „Synthesis of Heterocycles via Multicomponent Reactions I “
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.
Bibliographische Angaben
- 2010, XV, 280 Seiten, Maße: 16 x 24,1 cm, Gebunden, Englisch
- Herausgegeben: Romano V. A. Orru, Eelco Ruijter
- Verlag: Springer, Berlin
- ISBN-10: 364212674X
- ISBN-13: 9783642126741
- Erscheinungsdatum: 12.05.2010
Sprache:
Englisch
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