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A new paradigm for designing ring construction strategies for green organic synthesis: implications for the discovery of multicomponent reactions to build molecules containing a single ringA practical and efficient approach to imidazo[1,2-a]pyridine-fused isoquinolines through the post-GBB transformation strategy.Carbohydrates as a reagent in multicomponent reactions: one-pot access to a new library of hydrophilic substituted pyrimidine-fused heterocycles.Synthesis and preliminary biological evaluation of a small library of hybrid compounds based on Ugi isocyanide multicomponent reactions with a marine natural product scaffold.Application of Silica-Supported Alkylating Reagents in a One-Pot, Sequential Protocol to Diverse Benzoxathiazepine 1,1-Dioxides.Synergy Effects in the Chemical Synthesis and Extensions of Multicomponent Reactions (MCRs)-The Low Energy Way to Ultra-Short Syntheses of Tailor-Made Molecules.Unexpected isocyanide-based three-component bicyclization for the stereoselective synthesis of densely functionalized pyrano[3,4-c]pyrroles.Recent advances in the chemistry of metallated azetidines.Redox-Neutral Dual Functionalization of Electron-Deficient Alkenes.Stereoselective synthesis of fused tetrahydroquinazolines through one-pot double [3 + 2] dipolar cycloadditions followed by [5 + 1] annulation.Cascade bicyclization of triethylammonium thiolates with hydrazines: efficient access to pyrazolo[3,4-c]quinolines.Diastereoselective Synthesis of Cyclopenta[c]furans by a Catalytic Multicomponent Reaction.An Ugi Reaction Incorporating a Redox-Neutral Amine C-H Functionalization StepCuH-Catalyzed Regioselective Intramolecular Hydroamination for the Synthesis of Alkyl-Substituted Chiral Aziridines.Mechanochemical synthesis of small organic molecules.Diverse ring opening of thietanes and other cyclic sulfides: an electrophilic aryne activation approach.Synthesis of polyheterocycles via multicomponent reactions.New route for the synthesis of new cyanoimino- and cyanoaminopyrimidines.Synthesis of fluorescent heterocycles via a Knoevenagel/[4 + 1]-cycloaddition cascade using acetyl cyanide.Synthesis of functionalized dihydro-2-oxopyrroles using graphene oxide as heterogeneous catalyst.Efficient Access to Chiral Trisubstituted Aziridines via Catalytic Enantioselective Aza-Darzens Reactions.Transition metal-catalysed couplings between arenes and strained or reactive rings: combination of C-H activation and ring scission.Design, synthesis and fluorescence property evaluation of blue emitting triazole-linked chromene peptidomimetics.Domino ring-opening cyclization (DROC) of activated aziridines and epoxides with nitrones via dual-catalysis "on water".Copper(i)-Y zeolite catalyzed N-sulfonylketenimine mediated annulation of hydroxynaphthoquinones: syntheses of naphtho[2,1-b]furan-2,5-diones and benzo[de]chromene-2,6-diones.Metal-free cycloaddition to synthesize naphtho[2,3-d][1,2,3]triazole-4,9-diones.[Formula: see text]-catalyzed [Formula: see text] annulation between 3-oxirane-indolin-2-ones and nitrones to construct spiro[1,4,2-dioxazinan]oxindoles.A General, Concise Strategy that Enables Collective Total Syntheses of over 50 Protoberberine and Five Aporhoeadane Alkaloids within Four to Eight Steps.Bifunctional Furfuryl Cations Strategy: Three-Component Synthesis of Enamidyl Triazoles.Thiazine-2-thiones as Masked 1-Azadienes in Cascade Dimerization Reactions).In situ generation of nitrilium from nitrile ylide and the subsequent Mumm rearrangement: copper-catalyzed synthesis of unsymmetrical diacylglycine esters.One-pot synthesis of 1H-isochromenes and 1,2-dihydroisoquinolines by a sequential isocyanide-based multicomponent/Wittig reaction.Brook Rearrangement as a Trigger for the Ring Opening of Strained Carbocycles.A Four-Component Reaction for the Synthesis of Dioxadiazaborocines.A novel protocol for the facile construction of tetrahydroquinoline fused tricyclic frameworks via an intramolecular 1,3-dipolar nitrile oxide cycloaddition reaction.Stereoselective construction of functionalized tetracyclic and pentacyclic coumarinopyranpyrazole/pyrimidinedione/coumarin scaffolds using a solid-state melt reaction.Trityl Isocyanide as a Mechanistic Probe in Multicomponent Chemistry: Walking the Line between Ugi- and Strecker-type Reactions.Multicomponent mechanochemical synthesis.Mechanistic investigation of aziridine aldehyde-driven peptide macrocyclization: the imidoanhydride pathway.Multicomponent polysaccharide-protein bioconjugation in the development of antibacterial glycoconjugate vaccine candidates.
P2860
Q28817207-25A5DA03-7289-4B34-84A9-03F86C0A03D7Q33692158-32B70576-C06B-40DA-B143-ABACAE990EB8Q35333827-959BC047-C625-4F43-B3C9-8E25DCF273FCQ35793501-FA4E6473-8809-416E-8A3D-4D2D315910F5Q36051912-5A489B65-F346-42F5-B6D1-006FB72CEC47Q36293059-9C90549D-7504-4BF1-9717-101D7D5D91EBQ36436882-7BD097CC-4916-4DE0-9675-685F50ED74C5Q39003638-2D39B411-6FD8-4778-A3FD-395F802884C6Q41541098-472B42A5-3785-49BC-9C99-D8A277033241Q41593245-D1FFE594-5125-4129-AB15-A11AEE6DAFE3Q41689925-CFE4A918-ECD8-48F9-881E-B415A7DB2A42Q41861949-089345D1-6301-434C-AC24-2AFD9C98E8A9Q42154026-3A0A23FF-1CF5-4BE4-878C-96C601CC760EQ42631501-6ADC09C7-C896-4DF2-B078-B6F4EEBD1EB9Q43254790-ABF0911C-2FC2-4B90-AA21-137F938EDA52Q47241080-166DC0C9-9019-4836-B26B-35EBCDD7F9A1Q48121000-C8B6C394-E032-4B57-B9A2-51DD651F254DQ48147553-FBAFC2A5-450A-4C7F-A9AD-C65B09646E82Q48162528-5E94F09A-6F37-4489-A7AB-E07F6C7861F7Q48274364-EC241187-0C73-4DEB-8904-006A91D7CDD3Q48325519-BEAB70F7-0C99-4AAA-9E77-5BF59EEB4073Q49010401-D3844BF4-C8FD-427E-9411-FFBC12858449Q50176114-470B2C52-C4D9-4F16-AA8E-6EF7BD78549EQ50204495-536DF49E-C4AD-455E-B306-78ACEB82B825Q50225796-9BDE233F-0BC7-4139-A316-2733FEE09013Q50251139-CD498323-1070-4FED-8363-CE8C31EBD830Q50703457-46EBAFC1-A21D-404B-9CF1-29C1E01F4FF9Q50868632-4B472B33-2EE7-4355-B080-9B417802531DQ50907321-C43A7580-237E-40FC-8606-8EE9399F5ED4Q50942408-6518E276-C03C-4EBC-B146-A59429F70484Q51112075-4FCB52AF-805A-455A-8E60-6714050574D2Q51546552-1D832825-E972-473C-9CE3-C7A4B6EBECEAQ52895598-725B3CD5-7ECF-4F37-A102-29ED58B03F63Q53209817-C03AF7AC-BA0B-4789-89CC-712AB6BF10DCQ53379018-C1FFFB6D-6D8E-4954-B227-165668B859AFQ53526704-0132F987-A5BD-4E55-A57F-CC824425770DQ54382811-683E8398-A4EB-47D5-8712-E470B18BF8C7Q55281876-9CE58850-DDE4-4051-8A1B-F7F30E707443Q55292697-5D213824-6501-4533-B64F-D4E1DA02FA4DQ55331828-5A999D95-2AD3-475A-8D46-4CC135848B53
P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Small heterocycles in multicomponent reactions.
@en
type
label
Small heterocycles in multicomponent reactions.
@en
prefLabel
Small heterocycles in multicomponent reactions.
@en
P356
P1433
P1476
Small heterocycles in multicomponent reactions
@en
P2093
Andrei K Yudin
Serge Zaretsky
P304
P356
10.1021/CR400615V
P577
2014-07-17T00:00:00Z