Ruthenium-catalyzed azide-alkyne cycloaddition: scope and mechanism. - Wikidata - awgldk - TriplyDB

Ruthenium-catalyzed azide-alkyne cycloaddition: scope and mechanism.

Ruthenium-catalyzed azide-alkyne cycloaddition: scope and mechanism.

http://www.wikidata.org/entity/Q34788096

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Click chemistry in peptide-based drug design The click reaction as an efficient tool for the construction of macrocyclic structures Magnetically recoverable ruthenium catalysts in organic synthesis Braces for the peptide backbone: insights into structure-activity relationships of protease inhibitor mimics with locked amide conformations Generation of Candidate Ligands for Nicotinic Acetylcholine Receptors via in situ Click Chemistry with a Soluble Acetylcholine Binding Protein Template Design and synthesis of 4-(2,4,5-trifluorophenyl)butane-1,3-diamines as dipeptidyl peptidase IV inhibitors Kinetic target-guided synthesis in drug discovery and chemical biology: a comprehensive facts and figures survey Advances in Bioconjugation A cycloaddition route to novel triazole boronic esters An aldol-based build/couple/pair strategy for the synthesis of medium- and large-sized rings: discovery of macrocyclic histone deacetylase inhibitors.Copper(I)-catalyzed cycloaddition of organic azides and 1-iodoalkynes.Ynamides: a modern functional group for the new millennium.Recent development of two chitinase inhibitors, Argifin and Argadin, produced by soil microorganisms.Transition-metal-free catalytic synthesis of 1,5-diaryl-1,2,3-triazoles.Copper(I)-catalyzed cycloaddition of silver acetylides and azides: incorporation of volatile acetylenes into the triazole core.Preparation of 1,5-Disubstituted 1,2,3-Triazoles via Ruthenium-catalyzed Azide Alkyne Cycloaddition.A two-directional strategy for the diversity-oriented synthesis of macrocyclic scaffolds.Parallel solid-phase synthesis of diaryltriazoles.Probing the bioactive conformation of an archetypal natural product HDAC inhibitor with conformationally homogeneous triazole-modified cyclic tetrapeptides.64Cu-labeled somatostatin analogues conjugated with cross-bridged phosphonate-based chelators via strain-promoted click chemistry for PET imaging: in silico through in vivo studies Copper-catalyzed azide-alkyne cycloaddition (CuAAC) and beyond: new reactivity of copper(I) acetylides.Copper-catalyzed azide-alkyne cycloaddition: regioselective synthesis of 1,4,5-trisubstituted 1,2,3-triazoles.Ligand steric contours to understand the effects of N-heterocyclic carbene ligands on the reversal of regioselectivity in Ni-catalyzed reductive couplings of alkynes and aldehydes.Development of stable phosphohistidine analogues Click chemistry patents and their impact on drug discovery and chemical biology.Binaphthyl-1,2,3-triazole peptidomimetics with activity against Clostridium difficile and other pathogenic bacteria.Ruthenium-catalyzed cycloadditions of 1-haloalkynes with nitrile oxides and organic azides: synthesis of 4-haloisoxazoles and 5-halotriazoles.Mechanistic Basis for Regioselection and Regiodivergence in Nickel-Catalyzed Reductive Couplings Conformational properties of 1,4- and 1,5-substituted 1,2,3-triazole amino acids – building units for peptidic foldamers Transition metal-mediated synthesis of monocyclic aromatic heterocycles Integrated and passive 1,2,3-triazolyl groups in fluorescent indicators for zinc(II) ions: thermodynamic and kinetic evaluations Rhodium-catalyzed transannulation of 1,2,3-triazoles with nitriles.Palladium-Catalyzed C-H Arylation of 1,2,3-Triazoles.Click Chemistry and Radiochemistry: The First 10 Years Multi-component cycloaddition approaches in the catalytic asymmetric synthesis of alkaloid targets.A concomitant allylic azide rearrangement/intramolecular azide-alkyne cycloaddition sequence.Nitrogen-rich azoles as ligand spacers in coordination polymers.Catalytic selective synthesis.Beyond click chemistry - supramolecular interactions of 1,2,3-triazoles.Synthesis of triazole-nucleoside phosphoramidites and their use in solid-phase oligonucleotide synthesis.

P2860

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P2860

Ruthenium-catalyzed azide-alkyne cycloaddition: scope and mechanism.

http://www.wikidata.org/entity/Q34788096

description

2008 nî lūn-bûn

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2008 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2008 թվականի հունիսին հրատարակված գիտական հոդված

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2008年の論文

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年學術文章

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name

Ruthenium-catalyzed azide-alkyne cycloaddition: scope and mechanism.

@ast

Ruthenium-catalyzed azide-alkyne cycloaddition: scope and mechanism.

@en

Ruthenium-catalyzed azide-alkyne cycloaddition: scope and mechanism.

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type

label

Ruthenium-catalyzed azide-alkyne cycloaddition: scope and mechanism.

@ast

Ruthenium-catalyzed azide-alkyne cycloaddition: scope and mechanism.

@en

Ruthenium-catalyzed azide-alkyne cycloaddition: scope and mechanism.

@nl

prefLabel

Ruthenium-catalyzed azide-alkyne cycloaddition: scope and mechanism.

@ast

Ruthenium-catalyzed azide-alkyne cycloaddition: scope and mechanism.

@en

Ruthenium-catalyzed azide-alkyne cycloaddition: scope and mechanism.

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Journal of the American Chemical Society

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Ruthenium-catalyzed azide-alkyne cycloaddition: scope and mechanism.

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Brant C Boren

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Guochen Jia

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Lars K Rasmussen

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Li Zhang

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Sridhar Narayan

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8923-8930

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scholarly article

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10.1021/JA0749993

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130

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5284924

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18570425

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