Remotely controlled iridium-catalyzed asymmetric hydrogenation of terminal 1,1-diaryl alkenes.

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Neutral iridium catalysts with chiral phosphine-carboxy ligands for asymmetric hydrogenation of unsaturated carboxylic acids.Catalytic asymmetric hydrogenation of α-CF3- or β-CF3-substituted acrylic acids using rhodium(I) complexes with a combination of chiral and achiral ligands.

P2860

Q37741842-DED958E5-580C-414A-9500-87021D64A3D9 Q43877170-A206A16C-A643-429E-A86C-2EA1F6EFFA2C

P2860

Remotely controlled iridium-catalyzed asymmetric hydrogenation of terminal 1,1-diaryl alkenes.

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http://www.wikidata.org/entity/Q46966415

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2013 nî lūn-bûn

@nan

2013年の論文

@ja

2013年学术文章

@wuu

2013年学术文章

@zh

2013年学术文章

@zh-cn

2013年学术文章

@zh-hans

2013年学术文章

@zh-my

2013年学术文章

@zh-sg

2013年學術文章

@yue

2013年學術文章

@zh-hant

name

Remotely controlled iridium-ca ...... f terminal 1,1-diaryl alkenes.

@en

Remotely controlled iridium-ca ...... f terminal 1,1-diaryl alkenes.

@nl

type

Item

label

Remotely controlled iridium-ca ...... f terminal 1,1-diaryl alkenes.

@en

Remotely controlled iridium-ca ...... f terminal 1,1-diaryl alkenes.

@nl

prefLabel

Remotely controlled iridium-ca ...... f terminal 1,1-diaryl alkenes.

@en

Remotely controlled iridium-ca ...... f terminal 1,1-diaryl alkenes.

@nl

P1476

Remotely controlled iridium-ca ...... of terminal 1,1-diaryl alkenes

@en

P2093

Joost N H Reek

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

Rafael Gramage-Doria

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

P2860

Palladium-Catalyzed Ligand-Directed C−H Functionalization Reactions

Asymmetric Catalysis by Architectural and Functional Molecular Engineering: Practical Chemo- and Stereoselective Hydrogenation of Ketones

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

Asymmetric hydroboration of 1,1-disubstituted alkenes.

Asymmetric hydrogenation of alkenes lacking coordinating groups.

Catalytic homogeneous asymmetric hydrogenations of largely unfunctionalized alkenes.

Ir-catalysed asymmetric hydrogenation: Ligands, substrates and mechanism.

Iridium-catalyzed asymmetric hydrogenation of olefins.

BINOL-derived phosphoramidites in asymmetric hydrogenation: can the presence of a functionality in the amino group influence the catalytic outcome?

Asymmetric hydrogenation of minimally functionalised terminal olefins: an alternative sustainable and direct strategy for preparing enantioenriched hydrocarbons.

P304

8795-8797

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P31

scholarly article

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10.1002/ANIE.201302942

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

Tatiana Besset

P577

2013-07-24T00:00:00Z

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

P698

23893950

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

P921

Iriddjum

Remotely controlled iridium-catalyzed asymmetric hydrogenation of terminal 1,1-diaryl alkenes.

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P2860

P2860

Remotely controlled iridium-catalyzed asymmetric hydrogenation of terminal 1,1-diaryl alkenes.

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