First selective direct mono-arylation of piperidines using ruthenium-catalyzed C-H activation.

about

Ru-catalysed C-H arylation of indoles and pyrroles with boronic acids: scope and mechanistic studies α-Arylation of Saturated Azacycles and N-Methylamines via Palladium(II)-Catalyzed C(sp(3))-H Coupling.

P2860

Q35562633-B96A5FF2-1615-46F9-BD60-8A1C15BA0C38 Q39914728-C9567738-D78A-451E-8001-5AF8A894E67E

P2860

First selective direct mono-arylation of piperidines using ruthenium-catalyzed C-H activation.

Item

http://www.wikidata.org/entity/Q40745800

description

2013 nî lūn-bûn

@nan

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

2013年论文

@zh

2013年论文

@zh-cn

name

First selective direct mono-ar ...... nium-catalyzed C-H activation.

@en

type

Item

label

First selective direct mono-ar ...... nium-catalyzed C-H activation.

@en

prefLabel

First selective direct mono-ar ...... nium-catalyzed C-H activation.

@en

P1476

First selective direct mono-ar ...... enium-catalyzed C-H activation

@en

P2093

Maria C Schwarz

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

Navid Dastbaravardeh

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

P2860

Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density

Density-functional thermochemistry. III. The role of exact exchange

Understanding and exploiting C-H bond activation.

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

Pd(II)-catalyzed enantioselective C-H activation of cyclopropanes.

Mechanism of the rhodium(III)-catalyzed arylation of imines via C-H bond functionalization: inhibition by substrate.

Direct sp3 C-H bond activation adjacent to nitrogen in heterocycles.

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

Transition metal-catalyzed arylation of unactivated C(sp3)-H bonds.

Direct functionalization of (un)protected tetrahydroisoquinoline and isochroman under iron and copper catalysis: two metals, two mechanisms.

P2888

s00706-013-0947-1

P304

539-552

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

P31

scholarly article

P356

10.1007/S00706-013-0947-1

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

P433

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

P478

144

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

P50

Karl Kirchner

Michael Schnürch

Marko D. Mihovilovic

P577

2013-04-03T00:00:00Z

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

P5875

257450794

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

P698

26166880

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

P932

4494768

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

First selective direct mono-arylation of piperidines using ruthenium-catalyzed C-H activation.

about

P2860

P2860

First selective direct mono-arylation of piperidines using ruthenium-catalyzed C-H activation.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P932