Ligand-enabled ortho-C-H olefination of phenylacetic amides with unactivated alkenes.

about

Peptide-guided functionalization and macrocyclization of bioactive peptidosulfonamides by Pd(II)-catalyzed late-stage C-H activation

P2860

Q58714785-6FB98496-7BCB-4087-AB74-BC23F34E178F

P2860

Ligand-enabled ortho-C-H olefination of phenylacetic amides with unactivated alkenes.

Item

http://www.wikidata.org/entity/Q55019636

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh

2017年學術文章

@zh-hant

name

Ligand-enabled ortho-C-H olefination of phenylacetic amides with unactivated alkenes.

@en

Ligand-enabled ortho-C-H olefination of phenylacetic amides with unactivated alkenes.

@nl

type

Item

label

Ligand-enabled ortho-C-H olefination of phenylacetic amides with unactivated alkenes.

@en

Ligand-enabled ortho-C-H olefination of phenylacetic amides with unactivated alkenes.

@nl

prefLabel

Ligand-enabled ortho-C-H olefination of phenylacetic amides with unactivated alkenes.

@en

Ligand-enabled ortho-C-H olefination of phenylacetic amides with unactivated alkenes.

@nl

P1476

Ligand-enabled ortho-C-H olefination of phenylacetic amides with unactivated alkenes

@en

P2093

Hui Xu

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

Jin-Quan Yu

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

Ming-Zhu Lu

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

Xing-Rong Chen

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

P2860

Weak coordination as a powerful means for developing broadly useful C-H functionalization reactions.

Ligand-enabled reactivity and selectivity in a synthetically versatile aryl C-H olefination

Regioselective Intermolecular Coupling Reaction of Arylketones and Alkenes Involving C-H Bond Activation Catalyzed by an In-Situ Formed Cationic Ruthenium-Hydride Complex.

Pd(II)-catalyzed hydroxyl-directed C-H olefination enabled by monoprotected amino acid ligands.

Ligand-enabled meta-C-H activation using a transient mediator.

Rh(III)-catalyzed oxidative coupling of unactivated alkenes via C-H activation.

Ether-directed ortho-C-H olefination with a palladium(II)/monoprotected amino acid catalyst.

Palladium(II)-catalyzed C-H activation/C-C cross-coupling reactions: versatility and practicality.

Conformation-induced remote meta-C-H activation of amines.

Developing ligands for palladium(II)-catalyzed C-H functionalization: intimate dialogue between ligand and substrate.

P304

1311-1316

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

P31

scholarly article

P356

10.1039/C7SC04827K

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

P433

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

P478

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

P50

Hui-Xiong Dai

P577

2017-12-08T00:00:00Z

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

P698

29675177

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

P932

5887099

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

Ligand-enabled ortho-C-H olefination of phenylacetic amides with unactivated alkenes.

about

P2860

P2860

Ligand-enabled ortho-C-H olefination of phenylacetic amides with unactivated alkenes.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932