Maximizing synthetic efficiency: multi-component transformations lead the way
about
Identifying tumor cell growth inhibitors by combinatorial chemistry and zebrafish assaysUgi/Robinson–Gabriel reactions directed toward the synthesis of 2,4,5-trisubstituted oxazolesHigher-order multicomponent reactions: beyond four reactants.Strategies for innovation in multicomponent reaction design.Fluorous parallel synthesis of a piperazinedione-fused tricyclic compound libraryConstruction of a bicyclic beta-benzyloxy and beta-hydroxy amide library through a multicomponent cyclization reactionThree-component asymmetric catalytic Ugi reaction--concinnity from diversity by substrate-mediated catalyst assembly.A practical and efficient approach to imidazo[1,2-a]pyridine-fused isoquinolines through the post-GBB transformation strategy.Exploiting the Divalent Nature of Isonitriles: a novel Pictet-Spengler Amidination process.New tricks of well-known aminoazoles in isocyanide-based multicomponent reactions and antibacterial activity of the compounds synthesized.Design and discovery of novel monastrol-1,3,5-triazines as potent anti-breast cancer agent via attenuating Epidermal Growth Factor Receptor tyrosine kinase.Concise Two-Step Solution Phase Syntheses of four novel Dihydroquinazoline scaffolds.Two step syntheses of fused quinoxaline-benzodiazepines and bis-benzodiazepinesConcise Preparation of Novel Tricyclic Chemotypes: Fused Hydantoin-benzodiazepinesExpedient synthesis of a 72-membered isoxazolino-β-ketoamide library by a 2·3-component reaction.A tailor-made "tag-receptor" affinity pair for the purification of fusion proteins.Multicomponent macrocyclization reactions (MCMRs) employing highly reactive acyl ketene and nitrile oxide intermediates.Straightforward assembly of phenylimidazoquinoxalines via a one-pot two-step MCR processFacile, novel two-step syntheses of benzimidazoles, bis-benzimidazoles, and bis-benzimidazole-dihydroquinoxalines.Asymmetric multicomponent reactions (AMCRs): the new frontier.N-N bond formation in Ugi processes: from nitric acid to libraries of nitramines.Synergy Effects in the Chemical Synthesis and Extensions of Multicomponent Reactions (MCRs)-The Low Energy Way to Ultra-Short Syntheses of Tailor-Made Molecules.Multicomponent assembly of highly substituted indoles by dual palladium-catalyzed coupling reactionsChemo-differentiating ABB' multicomponent reactions. Privileged building blocks.Efficient and General Synthesis of 3-Aminoindolines and 3-Aminoindoles via Copper-Catalyzed Three Component Coupling ReactionMulti-component syntheses of heterocycles by transition-metal catalysis.Toward the Ideal Synthesis and Transformative Therapies: The Roles of Step Economy and Function Oriented Synthesis.Multicomponent synthesis of alpha-branched amides.One-pot synthesis of tetracyclic fused imidazo[1,2-a]pyridines via a three-component reaction.Recent progress of isocyanide-based multicomponent reactions in Iran.Multicomponent syntheses of functional chromophores.Ugi post-condensation copper-triggered oxidative cascade towards pyrazoles.Harnessing Thin-Film Continuous-Flow Assembly Lines.A one-pot multicomponent strategy for stereospecific construction of tricyclic pyrrolo[1,2-a]quinolines.Studies on the chemistry and reactivity of alpha-substituted ketones in isonitrile-based multicomponent reactionsStereochemical control of the Passerini reactionGeneral one-pot reductive gem-bis-alkylation of tertiary lactams/amides: rapid construction of 1-azaspirocycles and formal total synthesis of (±)-cephalotaxine.Pseudo-four component synthesis of mono- and di-benzylated-1,2,3-triazoles derived from aniline.Multi-component synthesis of peptide-sugar conjugates.One-pot syntheses of blue-luminescent 4-aryl-1H-benzo[f]isoindole-1,3(2H)-diones by T3P® activation of 3-arylpropiolic acids.
P2860
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P2860
Maximizing synthetic efficiency: multi-component transformations lead the way
description
2000 nî lūn-bûn
@nan
2000 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Maximizing synthetic efficiency: multi-component transformations lead the way
@ast
Maximizing synthetic efficiency: multi-component transformations lead the way
@en
type
label
Maximizing synthetic efficiency: multi-component transformations lead the way
@ast
Maximizing synthetic efficiency: multi-component transformations lead the way
@en
prefLabel
Maximizing synthetic efficiency: multi-component transformations lead the way
@ast
Maximizing synthetic efficiency: multi-component transformations lead the way
@en
P2093
P1476
Maximizing synthetic efficiency: multi-component transformations lead the way
@en
P2093
P304
P356
10.1002/1521-3765(20000915)6:18<3321::AID-CHEM3321>3.0.CO;2-A
P407
P577
2000-09-01T00:00:00Z