General method for functionalized polyaryl synthesis via aryne intermediates. - Test2 - elhamkhani - TriplyDB

General method for functionalized polyaryl synthesis via aryne intermediates.

General method for functionalized polyaryl synthesis via aryne intermediates.

http://www.wikidata.org/entity/Q34489853

about

Transition-Metal-Free C3 Arylation of Indoles with Aryl Halides.Synthesis of biaryls using aryne intermediates.Metal Free Bi(hetero)aryl Synthesis: A Benzyne Truce-Smiles Rearrangement Double heteroatom functionalization of arenes using benzyne three-component coupling.Development of a web-based platform for studying lithiation reactions in silico.Tandem Aryne-Capture/Sigmatropic Rearrangement as a Metal-Free Entry to Functionalized N-Aryl Pyrrolidines.Recent advances in fluoride-free aryne generation from arene precursors.

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P2860

General method for functionalized polyaryl synthesis via aryne intermediates.

http://www.wikidata.org/entity/Q34489853

description

2014 nî lūn-bûn

@nan

2014 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2014 թվականի հունիսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

General method for functionalized polyaryl synthesis via aryne intermediates.

@ast

General method for functionalized polyaryl synthesis via aryne intermediates.

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General method for functionalized polyaryl synthesis via aryne intermediates.

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type

label

General method for functionalized polyaryl synthesis via aryne intermediates.

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General method for functionalized polyaryl synthesis via aryne intermediates.

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General method for functionalized polyaryl synthesis via aryne intermediates.

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General method for functionalized polyaryl synthesis via aryne intermediates.

@ast

General method for functionalized polyaryl synthesis via aryne intermediates.

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General method for functionalized polyaryl synthesis via aryne intermediates.

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Journal of the American Chemical Society

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General method for functionalized polyaryl synthesis via aryne intermediates

@en

P2093

Ky Khac Anh Le

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Olafs Daugulis

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Thanh Truong

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P2860

Aryl-aryl bond formation one century after the discovery of the Ullmann reaction

Rhodium-catalyzed C-C bond formation via heteroatom-directed C-H bond activation.

Catalysts for Suzuki-Miyaura coupling processes: scope and studies of the effect of ligand structure.

One century of aryne chemistry.

Arynes and cyclohexyne in natural product synthesis.

Base-mediated intermolecular sp2 C-H bond arylation via benzyne intermediates.

Indolyne experimental and computational studies: synthetic applications and origins of selectivities of nucleophilic additions.

Transition-metal-catalyzed direct arylation of (hetero)arenes by C-H bond cleavage.

Cu-catalyzed arylation of phenols: synthesis of sterically hindered and heteroaryl diaryl ethers.

Steric effects compete with aryne distortion to control regioselectivities of nucleophilic additions to 3-silylarynes.

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8568-8576

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scholarly article

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10.1021/JA504886X

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2014-06-03T00:00:00Z

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