A homogeneous, recyclable polymer support for Rh(I)-catalyzed C-C bond formation. - Wikidata - awgldk - TriplyDB

A homogeneous, recyclable polymer support for Rh(I)-catalyzed C-C bond formation.

A homogeneous, recyclable polymer support for Rh(I)-catalyzed C-C bond formation.

http://www.wikidata.org/entity/Q35547047

about

Rh-catalyzed C-C cleavage of benzyl/allylic alcohols to produce benzyl/allylic amines or other alcohols by nucleophilic addition of intermediate rhodacycles to aldehydes and imines.Ir(COD)Cl]/Tris(2,4-di--butylphenyl)phosphite-Catalyzed Addition Reactions of Arylboronic Acids with Aldehydes

P2860

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P2860

A homogeneous, recyclable polymer support for Rh(I)-catalyzed C-C bond formation.

http://www.wikidata.org/entity/Q35547047

description

2011 nî lūn-bûn

@nan

2011 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2011年の論文

@ja

2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

name

A homogeneous, recyclable polymer support for Rh(I)-catalyzed C-C bond formation.

@ast

A homogeneous, recyclable polymer support for Rh(I)-catalyzed C-C bond formation.

@en

type

label

A homogeneous, recyclable polymer support for Rh(I)-catalyzed C-C bond formation.

@ast

A homogeneous, recyclable polymer support for Rh(I)-catalyzed C-C bond formation.

@en

prefLabel

A homogeneous, recyclable polymer support for Rh(I)-catalyzed C-C bond formation.

@ast

A homogeneous, recyclable polymer support for Rh(I)-catalyzed C-C bond formation.

@en

P1433

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P1433

Journal of Organic Chemistry

P1476

A homogeneous, recyclable polymer support for Rh(I)-catalyzed C-C bond formation.

@en

P2093

Jon A Tunge

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

Ranjan Jana

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

P2860

Hemilabile amidomonophosphine ligand-rhodium(I) complex-catalyzed asymmetric 1,4-addition of arylboronic acids to cycloalkenones.

Synthesis of stereodefined polysubstituted olefins. 1. Sequential intermolecular reactions involving selective, stepwise insertion of Pd(0) into allylic and vinylic halide bonds. The stereoselective synthesis of disubstituted olefins.

Solvent-free asymmetric olefin hydroformylation catalyzed by highly cross-linked polystyrene-supported (R,S)-BINAPHOS-Rh(I) complex.

Catalytic C-C bond formation via capture of hydrogenation intermediates.

Phase-trafficking reagents and phase-switching strategies for parallel synthesis.

The use of ultra- and nanofiltration techniques in homogeneous catalyst recycling.

Catalytic asymmetric approaches towards enantiomerically enriched diarylmethanols and diarylmethylamines.

A homogeneous, recyclable rhodium(I) catalyst for the hydroarylation of Michael acceptors.

Novel non-classical C9-methyl-5-substituted-2,4-diaminopyrrolo[2,3-d]pyrimidines as potential inhibitors of dihydrofolate reductase and as anti-opportunistic agents.

Practical asymmetric synthesis of a potent Cathepsin K inhibitor. Efficient palladium removal following Suzuki coupling.

P304

8376-8385

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P31

scholarly article

P356

10.1021/JO201476H

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P433

20

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P478

76

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2011-09-23T00:00:00Z

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51622459

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21895010

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3215106

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