: Maxim A. Mironov
: Maxim A. Mironov
: MCR 2009 Proceedings of the 4th International Conference on Multi-Component Reactions and Related Chemistry, Ekaterinburg, Russia
: Springer-Verlag
: 9781441972705
: Advances in Experimental Medicine and Biology
: 1
: CHF 193.20
:
: Organische Chemie
: English
: 230
: Wasserzeichen/DRM
: PC/MAC/eReader/Tablet
: PDF
Multi-component reactions warrant ever-increasing attention, as they are ideally suited for combinatorial synthesis (either on solid support or in solution) of libraries of products relevant to catalysis, such as agrochemicals or pharmaceuticals. Therefore, the study and implementation of MCRs possesses a wide range of appeal and applicability. A broad and expanding audience of scientists and students continues to apply the concepts of multi-component chemistry to an array of disciplines-this collection of research offers an angle for each and brings together the vast scope of possibilities within the greater community.

Maxim A. Mironov is affiliated with Ural State Technical University, Ekaterinburg, Russian Federation
Contents6
Introduction to the Proceedings of the Fourth International Conference on Multi-Component Reactions and Related Chemistry8
Session 1: Catalysis and Multi-Component Reactions12
Recent Progress in Asymmetric Two-Center Catalysis13
Efficiency in Chemistry: From Hydrogen Autotransfer to Multi-component Catalysts15
Multi-component Reactions by Microwave-Assisted, Continuous Flow Organic Synthesis16
A Potpourri of Recent Microwave-Assisted 2(1H)-Pyrazinone Chemistry18
Efficient Construction of (Hetero)Aryl Substituted (Aza)Indoles by Pd-Catalyzed Multi-component Reactions20
Chlorotrimethylsilane is an Efficient Promoter for the Biginelli Reaction22
Three-Component Synthesis of Dihydropyrimidobenzimidazol Derivatives in the Presence of MgO as a Highly Effective Heterogeneous Base Catalyst22
2422
[Hmim]TFA-Catalyzed Multi-component Reaction: Direct, Mild, and Efficient Procedure for the Synthesis of 1,2-Dihydroquinazolines22
2622
Synthesis of Benzofurans Catalyzed by 1,4-Diazabicyclo[2,2,2]Octane in Solventless System28
Silica Sulfuric Acid: Highly Efficient Catalyst for the Synthesis of Imidazo[1,2-a]pyridines Using Trimethylsilylcyanide or Cyanohydrins28
2928
Efficient Construction of (Aza)Indolyl Ynones by Pd/Cu-Catalyzed Multi-component Reactions31
Multi-component Synthesis of Pyridazine and Pyridazinoquinazoline Derivatives in the Presence of 12-Tungstophosphoric Acid33
Research of Nanosized Metal Oxide Action on Regio- and Stereoselectivity of the Multi-component Hantzsch Reaction35
Nanocrystalline Copper (II) Oxide-Catalyzed One-pot Synthesis of Polyfunctionalized Pyrans via a Three-Component Cyclocondensation35
Nanocrystalline Copper (II) Oxide-Catalyzed One-pot Synthesis of Polyfunctionalized Pyrans via a Three-Component Cyclocondensation35
3835
Reference14
Session 2: Multi-Component Reactions in Heterocyclic Chemistry39
Multi-component Synthesis of Heterocycles by Palladium-catalyzed Generation of Alkynones, Alkenones and Allenes40
Multi-component Reactions as Useful Platforms to Explore the Chemical Space42
Multi-component Heterocyclizations: Control of Chemo- and Regioselectivity44
Multi-component Reactions of H2S with Aldehydes and Amines as an Efficient Route to Heterocycles and Thioaza-Crown Compounds46
Cascade Recyclizations of 1H-Pyrrole-2, 3-diones: A Method of Unusual Heterocyclic Systems Construction49
Alkyne-Induced Tandem Transformations of (Hetero)Annulated Five-, Six-, or Seven-Membered N-Heterocycles and a New MCR on This Motif49
5149
N C and C C Recyclizations of Pyrimidinium Salts53
Synthetic Approach to Highly Functionalized Mesocyclic Heterocycles by Coupling an Ugi or Passerini Reaction (PADAM Strategy) with a Pd-Mediated Cyclocarbonylation53
5553
Solvent-Free Three-Component Condensation of Aldehydes and Malononitrile with Naphthols Affording 2-Amino-4H-chromenes57
General Procedure for 2-Amino-4H-Chromenes57
New Pyrido[3,2-c]pyridones and Pyrido[3,2-c]pyrazoles Accessible by a One-Step Multi-component Synthesis59
Synthesis of 1-Hydroxyaryl-4-Acyl-5-Aryl-3-Hydroxy-3-Pyrrolin-2-Ones61
Synthesis of Highly Stable, Unusual Charge-Separated Pyridinium-, Isoquinolinium-, Quinolinium-, and N-Methylimidazolium-Tetronic Acid Zwitterions61
6361
Synthesis of 4(5)-Imidazolecarboxylic Acid Derivatives64
Polyfunctional U-MCR Reagents: Convenient Pathway to Novel Heterocyclic Systems67
One-Pot Synthesis of Pyridines by Cyclocondensation of Acetyl- and Benzoylpyruvates, Trimethyl Orthoformate, and Enamines69
Unprecedented Multi-component Approach to 1,4-Diazepine- and 1,4-Benzodiazepine Ring Formation71
Synthesis and Interaction with Butylamine of Methyl 6-Acyl-7-Phenyl-4,7-Dihydrotetrazolo[1,5-a]Pyrimidine-5-Carboxylates72
One-Pot Synthesis of 5-Oxo-1,3,4,5-Tetrahydro-Pyrrolo[4,3,2-de]Isoquinoline-3-Carboxamides74
Synthesis of 4-Acyl-5-Aryl-1-(2,2-dimethoxyethyl)-3-Hydroxy-3-Pyrrolin-2-Ones76
Synthesis and Structure of Isopropyl 5-Methyl-7-aryl-4,7-Dihydrotetrazolo[1,5-a]Pyrymidine-6-Carboxylates78
References41
Session 3: Multi-Component Reactions in Drug Discovery80
Multi-component Reactions and Drug Discovery83
Building Molecular Shape Diversity via Post-Ugi Annulations84
A Fast and Efficient Approach to Small Molecular Weight Protein-Protein Interaction Antagonists Using MCR Chemistry86
Molecular Diversification and Solid-Phase Synthesis of N-Acylpeptides for Antibiotic Screening88
Convertible Products of Ugi Reaction Involving Azole Carboxylic Acids and tert-Butyl Isocyanide90
Applications of Quinoxaline Synthesis via Isocyanide-Based MCR92
Continued Evidence for the Utility of TMSCl as Promoter for Groebke-Blackburn Reactions: Synthesis of Imidazo[2,1-b][1,3]benzothiazoles92
9492
Systematic Diversity-Oriented Synthesis Based on Ugi Reaction Products96
Priaxon AG, a New Dimension in Drug Discovery99
Isocyanide-Based Multi-component Reaction of Diamines: An Efficient Strategy for Assembling of Unique Heterocyclic Scaffolds100
A Convenient Synthesis of Novel Heterocyclic Structures Containing 11-Oxo-6,11,12,13-tetrahydrodibenzo[b,g][1,5]oxazonine Fragment100
101100
Synthesis of Substituted 3-Methyl-1-oxo-2,3,4,5-tetrahydro-1H-benzo[C]azepino-3-carboxamides103
New Approach of Some Bifunctional Initials in U-4MCR105
One-Step Assembly of Novel Carbamoyl-Substituted Heterocycle-Fused 1-Oxo-2,3-dihydro-1H-benzo[c]azepines106
A Facile One-Pot Greener Synthesis and Antibacterial Activity of 2-Amino-4H-pyran Derivatives108
Session 4: Novel Reagents for Multi-Component Reactions109
Pluripotent Substrates in Diversity-Oriented Synthesis112
New Polyfunctional Reagents for Isocyanide-Based Multi-component Reactions114
Products of Ugi Reaction Among Acid Hydrazides, Aldehydes, and Isocyanides with Added Diversity116
Highly Functionalized Tricyclic N-Heterocycles by Coupling an Ugi MCR with a Tandem Pd(0)-Promoted SN2'-Heck Reaction116
118116
Cascade Transformations of N-(1-Aryl-2-polychloroethyl)sulfonamides120
New Strategy for the Synthesis of Fluorinated Compounds: Multi-component Reactions Including Fluoro-containing Building Blocks122
A Multi-component Reaction Leading to a Phenalenone Derivative124
Heteropoly Acids in One-Pot, Three-Component Synthesis of 4-Aminoquinazolines125
Passerini Multi-component Reaction of Indane-1,2,3-trione, Isocyanides and 2-Furancarboxylic Acid127
A Novel Route to the Synthesis of Fluoroalkylated Hexahydroimidazo[1,2-a]Pyridines128
Exploiting the Secondary Amines and the Glycolaldehyde Dimer in the Ugi Reaction: Formation of a Novel Passerini Ugi Chimera Scaffold128
130128
Three-Component Synthesis of 4´H-spiro [Adamantane-2,3´-isoqunolines]131
Nonracemizable Isocyanoacetates for Multi-component Reactions133
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