Bis(dibenzylideneacetone)palladium(0) - Wikidata - wikimedia - TriplyDB

Bis(dibenzylideneacetone)palladium(0)

Bis(dibenzylideneacetone)palladium(0)

http://www.wikidata.org/entity/Q29398389

about

Bis(dibenzylideneacetone)palladium(0)

http://www.wikidata.org/entity/Q29398389

description

2013 nî lūn-bûn

@nan

2013 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

name

Bis(dibenzylideneacetone)palladium(0)

@ast

Bis(dibenzylideneacetone)palladium(0)

@en

type

label

Bis(dibenzylideneacetone)palladium(0)

@ast

Bis(dibenzylideneacetone)palladium(0)

@en

prefLabel

Bis(dibenzylideneacetone)palladium(0)

@ast

Bis(dibenzylideneacetone)palladium(0)

@en

P1433

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P1476

Q29398389-6B4EEFDF-AF89-4F88-80E8-6CDD7711130C

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P2860

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P356

047084289X.RB138.PUB3

P1433

Encyclopedia of Reagents for Organic Synthesis

P1476

Bis(dibenzylideneacetone)palladium(0)

@en

P2093

Adrian Ortiz

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

Christopher S. Regens

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

F. Christopher Pigge

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

John R. Stille

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

Ke Chen

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

Martin D. Eastgate

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

P2860

Alkyne elementometalation-Pd-catalyzed cross-coupling. Toward synthesis of all conceivable types of acyclic alkenes in high yields, efficiently, selectively, economically, and safely: "green" way

Palladium-Catalyzed C−O Coupling Involving Unactivated Aryl Halides. Sterically Induced Reductive Elimination To Form the C−O Bond in Diaryl Ethers

Palladium-catalyzed intramolecular delta-lactam formation of aryl halides and amide-enolates: syntheses of cherylline and latifine.

Oxidative transformation of tert-cyclobutanols by palladium catalysis under oxygen atmosphere.

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

Design and implementation of new, silicon-based, cross-coupling reactions: importance of silicon-oxygen bonds.

Palladium oxidase catalysis: selective oxidation of organic chemicals by direct dioxygen-coupled turnover.

Palladium(0)-catalyzed intermolecular amination of unactivated C(sp³)-H bonds.

Synthesis of (+)-CP-99,994 via Pd(0)-catalyzed asymmetric allylic and homoallylic C-H Diamination of terminal olefin.

Catalytic asymmetric allylic and homoallylic diamination of terminal olefins via formal C-H activation

P31

scholarly article

P356

10.1002/047084289X.RB138.PUB3

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

P577

2013-04-22T00:00:00Z

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