Isocyanide-based multicomponent reactions towards cyclic constrained peptidomimetics.
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Isocyanide-Based Multicomponent Reactions for the Synthesis of HeterocyclesSynthesis of antibacterial 1,3-diyne-linked peptoids from an Ugi-4CR/Glaser coupling approachA practical and efficient approach to imidazo[1,2-a]pyridine-fused isoquinolines through the post-GBB transformation strategy.New tricks of well-known aminoazoles in isocyanide-based multicomponent reactions and antibacterial activity of the compounds synthesized.Efficient synthesis of conformationally constrained, amino-triazoloazepinone-containing di- and tripeptides via a one-pot Ugi-Huisgen tandem reaction.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.One-pot synthesis of tetracyclic fused imidazo[1,2-a]pyridines via a three-component reaction.Metal-mediated post-Ugi transformations for the construction of diverse heterocyclic scaffolds.Review cyclic peptides on a merry-go-round; towards drug design.Multicomponent syntheses of functional chromophores.Application of the Ugi reaction with multiple amino acid-derived components: synthesis and conformational evaluation of piperazine-based minimalist peptidomimetics.Sulfur-Switch Ugi Reaction for Macrocyclic Disulfide-Bridged Peptidomimetics.Cysteine Isocyanide in Multicomponent Reaction: Synthesis of Peptido-Mimetic 1,3-Azoles.Stereoselective Synthesis of Functionalized Bicyclic Scaffolds by Passerini 3-Center-2-Component Reactions of Cyclic Ketoacids.Concise Synthesis of Tetrazole MacrocycleN-Hydroxyimide Ugi Reaction toward α-Hydrazino Amides.Mechanochemical synthesis of small organic molecules.With unprotected amino acids to tetrazolo peptidomimetics.Two-Step Synthesis of Complex Artificial Macrocyclic Compounds.Direct access to isoxazolino and isoxazolo benzazepines from 2-((hydroxyimino)methyl)benzoic acid via a post-Ugi heteroannulation.Two-Step Macrocycle Synthesis by Classical Ugi Reaction.β-Lactam Synthesis through Diodomethane Addition to Amide Dianions.A multicomponent conjugation strategy to unique N-steroidal peptides: first evidence of the steroidal nucleus as a β-turn inducer in acyclic peptides.Efficient one-pot synthesis of amino-benzotriazolodiazocinone scaffolds via catalyst-free tandem Ugi-Huisgen reactions.Trityl Isocyanide as a Mechanistic Probe in Multicomponent Chemistry: Walking the Line between Ugi- and Strecker-type Reactions.Methyl isocyanide as a convertible functional group for the synthesis of spirocyclic oxindole γ-lactams via post-Ugi-4CR/transamidation/cyclization in a one-pot, three-step sequence.Mechanistic investigation of aziridine aldehyde-driven peptide macrocyclization: the imidoanhydride pathway.Hexafluoroisopropanol as the Acid Component in the Passerini Reaction: One-Pot Access to β-Amino Alcohols.Isocyanide-based multicomponent reactions in the synthesis of heterocyclesExploitation of the Ugi 5-Center-4-Component Reaction (U-5C-4CR) for the Generation of Diverse Libraries of Polycyclic (Spiro)Compounds
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P2860
Isocyanide-based multicomponent reactions towards cyclic constrained peptidomimetics.
description
article científic
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article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
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artículo científico
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name
Isocyanide-based multicomponent reactions towards cyclic constrained peptidomimetics.
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type
label
Isocyanide-based multicomponent reactions towards cyclic constrained peptidomimetics.
@en
prefLabel
Isocyanide-based multicomponent reactions towards cyclic constrained peptidomimetics.
@en
P2860
P356
P1476
Isocyanide-based multicomponent reactions towards cyclic constrained peptidomimetics
@en
P2093
Gijs Koopmanschap
P2860
P304
P356
10.3762/BJOC.10.50
P577
2014-03-04T00:00:00Z