Ugi/Robinson–Gabriel reactions directed toward the synthesis of 2,4,5-trisubstituted oxazoles - Test2 - elhamkhani - TriplyDB

Ugi/Robinson–Gabriel reactions directed toward the synthesis of 2,4,5-trisubstituted oxazoles

Ugi/Robinson–Gabriel reactions directed toward the synthesis of 2,4,5-trisubstituted oxazoles

http://www.wikidata.org/entity/Q24597154

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Exploiting the Divalent Nature of Isonitriles: a novel Pictet-Spengler Amidination process.Hydrazine-mediated cyclization of Ugi products to synthesize novel 3-hydroxypyrazoles Isocyanide-based multicomponent reactions towards cyclic constrained peptidomimetics.Development of a method for the synthesis of 2,4,5-trisubstituted oxazoles composed of carboxylic acid, amino acid, and boronic acid.Tertiary amines as synthetic equivalents of vinyl cations: zinc bromide promoted coupling of propargylamines with α-isocyanoacetamides to give 2,4,5-trisubstituted oxazoles initiated by an internal redox process.Reaction of alkynes and azides: not triazoles through copper-acetylides but oxazoles through copper-nitrene intermediates.Synthesis of isoindolin-1-one derivatives via multicomponent reactions of methyl 2-formylbenzoate and intramolecular amidation.

P2860

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P2860

Ugi/Robinson–Gabriel reactions directed toward the synthesis of 2,4,5-trisubstituted oxazoles

http://www.wikidata.org/entity/Q24597154

description

2012 nî lūn-bûn

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2012 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2012 թվականի ապրիլին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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Ugi/Robinson–Gabriel reactions ...... 2,4,5-trisubstituted oxazoles

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Ugi/Robinson–Gabriel reactions ...... 2,4,5-trisubstituted oxazoles

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Ugi/Robinson–Gabriel reactions ...... 2,4,5-trisubstituted oxazoles

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Ugi/Robinson–Gabriel reactions ...... 2,4,5-trisubstituted oxazoles

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Ugi/Robinson–Gabriel reactions ...... 2,4,5-trisubstituted oxazoles

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Ugi/Robinson–Gabriel reactions ...... 2,4,5-trisubstituted oxazoles

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Ugi/Robinson–Gabriel reactions ...... 2,4,5-trisubstituted oxazoles

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Ugi/Robinson–Gabriel reactions ...... 2,4,5-trisubstituted oxazoles

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Ugi/Robinson–Gabriel reactions ...... 2,4,5-trisubstituted oxazoles

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J.TETLET.2012.02.030

P1433

Tetrahedron Letters

P1476

Ugi/Robinson–Gabriel reactions ...... 2,4,5-trisubstituted oxazoles

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P2093

Arthur Y Shaw

http://www.w3.org/2001/XMLSchema#string

Christopher Hulme

http://www.w3.org/2001/XMLSchema#string

Zhigang Xu

http://www.w3.org/2001/XMLSchema#string

P2860

One-pot Friedel-Crafts/Robinson-Gabriel synthesis of oxazoles using oxazolone templates

Maximizing synthetic efficiency: multi-component transformations lead the way

"Multi-component reactions : emerging chemistry in drug discovery" 'from xylocain to crixivan'.

Rapid assembly of molecular diversity via exploitation of isocyanide-based multi-component reactions.

Design, synthesis, and biological evaluation of the combinatorial library with a new spirodiketopiperazine scaffold. Discovery of novel potent and selective low-molecular-weight CCR5 antagonists.

Emerging approaches for the syntheses of bicyclic imidazo[1,2-x]-heterocycles.

1,4-Thienodiazepine-2,5-diones via MCR (II): scaffold hopping by Gewald and Ugi-deprotection-cyclization strategy

Recent developments in isocyanide based multicomponent reactions in applied chemistry.

Isocyanide-based multicomponent reactions in drug discovery.

A direct synthesis of oxazoles from aldehydes.

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1998-2000

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scholarly article

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10.1016/J.TETLET.2012.02.030

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15

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53

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2012-04-11T00:00:00Z

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236114914

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23559684

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Aagianik kimischri

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3613284

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