Aryl-Aryl Bond Formation by the Fluoride-Free Cross-Coupling of Aryldisiloxanes with Aryl Bromides

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Mechanism of the Transmetalation of Organosilanes to Gold.Pd-catalyzed synthesis of symmetrical and unsymmetrical siloxanes.Palladium-Catalysed Cross-Coupling of Vinyldisiloxanes with Benzylic and Allylic Halides and Sulfonates

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Q37000771-75603CAA-C2C1-42CC-9E01-9EC7EFFA76AB Q44200656-262F5C18-AF7E-4273-8976-F20ACCC1AFBE Q57540653-AC30974E-4836-45F4-A22D-D9CDE9BC84ED

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Aryl-Aryl Bond Formation by the Fluoride-Free Cross-Coupling of Aryldisiloxanes with Aryl Bromides

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http://www.wikidata.org/entity/Q57540669

description

article

@en

im Oktober 2011 veröffentlichter wissenschaftlicher Artikel

@de

wetenschappelijk artikel

@nl

наукова стаття, опублікована в жовтні 2011

@uk

name

Aryl-Aryl Bond Formation by th ...... disiloxanes with Aryl Bromides

@en

Aryl-Aryl Bond Formation by th ...... disiloxanes with Aryl Bromides

@nl

type

Item

label

Aryl-Aryl Bond Formation by th ...... disiloxanes with Aryl Bromides

@en

Aryl-Aryl Bond Formation by th ...... disiloxanes with Aryl Bromides

@nl

prefLabel

Aryl-Aryl Bond Formation by th ...... disiloxanes with Aryl Bromides

@en

Aryl-Aryl Bond Formation by th ...... disiloxanes with Aryl Bromides

@nl

P1476

Aryl-aryl bond formation by th ...... disiloxanes with aryl bromides

@en

P2093

Christine M Boehner

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

Claire Crawford

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

David Norton

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

Elizabeth C Frye

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

Gillian Turner

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

Hannah F Sore

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

Helen Horsley

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

Kieron M G O'Connell

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

Martin Owen

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

Patricia Garcia Dominguez

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

P2860

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

Biaryl Phosphane Ligands in Palladium-Catalyzed Amination

Diversity-oriented synthesis as a tool for the discovery of novel biologically active small molecules.

Organotrifluoroborates: protected boronic acids that expand the versatility of the Suzuki coupling reaction.

Cross-coupling reactions of organosilicon compounds: new concepts and recent advances.

Application of statistical 'design of experiments' methods in drug discovery.

The interplay of invention, discovery, development, and application in organic synthetic methodology: a case study.

Cross-coupling reactions of aromatic and heteroaromatic silanolates with aromatic and heteroaromatic halides.

Vinylation of aromatic halides using inexpensive organosilicon reagents. Illustration of design of experiment protocols.

Recent advances in aryl-aryl bond formation by direct arylation.

P304

13230-13239

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

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scholarly article

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10.1002/CHEM.201102285

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

P407

English

P433

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

P478

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

P50

David R. Spring

David G Hulcoop

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2011-10-11T00:00:00Z

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

P698

21990071

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P921

general chemistry

Aryl-Aryl Bond Formation by the Fluoride-Free Cross-Coupling of Aryldisiloxanes with Aryl Bromides

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P2860

P2860

Aryl-Aryl Bond Formation by the Fluoride-Free Cross-Coupling of Aryldisiloxanes with Aryl Bromides

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921