Higher-order multicomponent reactions: beyond four reactants.
about
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 ringMethionine and seleno-methionine type peptide and peptoid building blocks synthesized by five-component five-center reactions.Highly stereoselective synthesis of natural-product-like hybrids by an organocatalytic/multicomponent reaction sequence.Diastereoselective three-component synthesis of β-amino carbonyl compounds using diazo compounds, boranes, and acyl imines under catalyst-free conditions.Exploiting the Divalent Nature of Isonitriles: a novel Pictet-Spengler Amidination process.Rapid, scalable assembly of stereochemically rich, mono- and bicyclic acyl sultamsCarbohydrates as a reagent in multicomponent reactions: one-pot access to a new library of hydrophilic substituted pyrimidine-fused heterocycles.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.Multicomponent reactions in nucleoside chemistry.Hyperbranched polymers: advances from synthesis to applications.Multicomponent syntheses of functional chromophores.Domino reaction of arylglyoxals with pyrazol-5-amines: selective access to pyrazolo-fused 1,7-naphthyridines, 1,3-diazocanes, and pyrroles.Four-component strategy for selective synthesis of azepino[5,4,3-cd]indoles and pyrazolo[3,4-b]pyridinesMicrowave-assisted Cu(I)-catalyzed, three-component synthesis of 2-(4-((1-phenyl-1H-1,2,3-triazol-4-yl)methoxy)phenyl)-1H-benzo[d]imidazoles.Stereoselective synthesis of fused tetrahydroquinazolines through one-pot double [3 + 2] dipolar cycloadditions followed by [5 + 1] annulation.The Flögel-three-component reaction with dicarboxylic acids - an approach to bis(β-alkoxy-β-ketoenamides) for the synthesis of complex pyridine and pyrimidine derivatives.Synthesis of structurally diverse 3,4-dihydropyrimidin-2(1H)-ones via sequential Biginelli and Passerini reactions.Multicomponent versus domino reactions: One-pot free-radical synthesis of β-amino-ethers and β-amino-alcohols.Enantioselective Multicomponent Condensation Reactions of Phenols, Aldehydes, and Boronates Catalyzed by Chiral Biphenols.Mechanochemical synthesis of small organic molecules.Highly efficient four-component synthesis of 4(3H)-quinazolinones: palladium-catalyzed carbonylative coupling reactions.Enantioselective organocatalytic multicomponent synthesis of 2,6-diazabicyclo[2.2.2]octanones.One-pot formation of fluorescent γ-lactams having an α-phosphorus ylide moiety through three-component α(δ')-Michael reactions of phosphines with an enyne and N-tosyl aldimines.Pseudo-four component synthesis of mono- and di-benzylated-1,2,3-triazoles derived from aniline.One-pot syntheses of blue-luminescent 4-aryl-1H-benzo[f]isoindole-1,3(2H)-diones by T3P® activation of 3-arylpropiolic acids.Multicomponent reactions of phosphines, enynedioates and benzylidene malononitriles generated highly substituted cyclopentenes through an unexpected phosphine α-addition-δ-evolvement of an anion pathway.Transition metal-catalyzed C-H bond functionalization in multicomponent reactions: a tool toward molecular diversity.Synthesis of disulfides tethered pyrroles from β-ketothioamides via a bicyclization/ring-opening/oxidative coupling reaction.With unprotected amino acids to tetrazolo peptidomimetics.Copper(i) catalyzed oxidative hydrolysis of Ugi 3-component and Ugi-azide reaction products towards 2° α-ketoamides and α-ketotetrazoles.Diastereoselective synthesis of tetrahydropyrans via Prins-Ritter and Prins-arylthiolation cyclization reactions.Two-Step Macrocycle Synthesis by Classical Ugi Reaction.A Four-Component Reaction Strategy for Pyrimidine Carboxamide Synthesis.Construction of Tropane Derivatives by the Organocatalytic Asymmetric Dearomatization of Isoquinolines.I2 catalyzed access of spiro[indoline-3,4'-pyridine] appended amine dyad: new ON-OFF chemosensors for Cu2+ and imaging in living cells.A tunable copper-catalyzed multicomponent reaction towards alkaloid-inspired indole/lactam polycycles.A General, Concise Strategy that Enables Collective Total Syntheses of over 50 Protoberberine and Five Aporhoeadane Alkaloids within Four to Eight Steps.Spin-labelled diketopiperazines and peptide-peptoid chimera by Ugi-multi-component-reactions.Exploring Ugi-Azide Four-Component Reaction Products for Broad-Spectrum Influenza Antivirals with a High Genetic Barrier to Drug Resistance.
P2860
Q28817207-DFA3EE40-CEF5-4CB9-B0D9-0ADC504EC195Q30313327-1D8942BA-D586-4676-937F-C2CC438B794FQ30316563-C4FFD1DB-B7B8-4017-BA23-2EFB91740A78Q33662369-4FA992F9-16EF-461B-B6D9-DBD008BA5992Q33773093-41571799-2A0D-4F84-B286-E394EDE6BF74Q35061640-4631475D-7DBC-49E0-83AB-FB3F7ED75FF4Q35333827-CC724B71-843B-43F7-A1D5-04C9A9837798Q36293059-52AD01B2-5047-454F-AA9D-DB7B6033EE13Q36436882-897E36B6-6905-45A7-9264-D0C106D53DF3Q38243795-FD7F3DE8-AE90-43C9-94FC-0850EF581BF2Q38435973-F53C9343-1478-4A7E-B0D9-72D193A439D5Q38742514-56B897F8-5E19-471D-B372-8FB224D21477Q40759300-96A980AB-BE51-4F99-B6D8-5120F400611DQ40787385-AE6347B5-1601-46B1-8F2B-2984FBAFC3A7Q41586281-AF148312-6834-4D78-A9F6-B09AA61B3E4FQ41593245-F9C69086-8FA5-4539-9DE9-570433B481A6Q42001141-ED3036BE-416C-44D4-9516-76E20E809B59Q42134384-432EBE4F-05FF-4C70-9037-743B0F922958Q43124361-65D93400-2CC3-419C-8934-83521B88BAE0Q43141595-66D050D7-0E5A-4326-8B09-7009D8F54777Q43254790-CF8FFE0A-2AD3-45BE-BAE9-0F39B1AE4C56Q43864737-1DD9D4FC-7E6E-4E71-A90E-18D3D5B45ED0Q43987619-1D5D6BB0-3352-4B33-B1A9-7A55F24479C9Q44560502-D9DC0FE8-710E-4033-B889-BC0F41D92070Q44595432-11BE6596-4593-4219-A805-D6C31CDC5093Q45996876-60A0096C-02C5-4359-A0FE-55D7A7961345Q46605659-818647F5-688E-45C6-956C-6F6C37ED424FQ47405673-219D8029-E698-424B-9132-88164A024D64Q47975003-B8B1D730-3203-4B75-B9D2-B9F44AD1F0D1Q48126099-215A0318-F527-40D9-B9B8-250A47B6F8CEQ48166895-E1F0E4C1-4955-4880-9918-3195E5699BD0Q48253424-1A9C7BBB-5750-41F6-B29A-6879DF10B64DQ48254415-F5E3FFC9-9D3F-44BA-8092-6A7F4B3DFDEDQ48902737-10C9F032-6D76-4B3C-B38A-32CC0A18C6AAQ49064904-0F760326-7039-4F23-9C77-FB20F63AF3A2Q49829064-4D276208-4585-43EE-8915-EDF9492F9C15Q50666452-3288508C-FA03-4F2F-B7DA-8E40AEED42A3Q50868632-DFC62974-C384-409B-973C-3076AF72EC2CQ51050621-FF48D917-09AB-42E2-9FE9-E3F9717E0A11Q51783651-7D1DEE31-50C7-4A9C-9515-A5AC0043F5F1
P2860
Higher-order multicomponent reactions: beyond four reactants.
description
2013 nî lūn-bûn
@nan
2013 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Higher-order multicomponent reactions: beyond four reactants.
@ast
Higher-order multicomponent reactions: beyond four reactants.
@en
type
label
Higher-order multicomponent reactions: beyond four reactants.
@ast
Higher-order multicomponent reactions: beyond four reactants.
@en
prefLabel
Higher-order multicomponent reactions: beyond four reactants.
@ast
Higher-order multicomponent reactions: beyond four reactants.
@en
P2093
P2860
P356
P1476
Higher-order multicomponent reactions: beyond four reactants.
@en
P2093
Bernhard Westermann
Sander S van Berkel
Sebastian Brauch
P2860
P304
P356
10.1039/C3CS35505E
P577
2013-06-01T00:00:00Z