Highly enantioselective asymmetric transfer hydrogenation (ATH) of α-phthalimide ketones.

about

The Development of Phosphine-Free "Tethered" Ruthenium(II) Catalysts for the Asymmetric Reduction of Ketones and Imines.Chiral-at-metal iridium complex for efficient enantioselective transfer hydrogenation of ketones.

P2860

Q38927774-AD8AFE7C-51AE-4EF6-9138-803C2178C5DD Q51497139-CDDA2090-9AFB-4874-9B98-68F4EE61EDED

P2860

Highly enantioselective asymmetric transfer hydrogenation (ATH) of α-phthalimide ketones.

Item

http://www.wikidata.org/entity/Q53657078

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年学术文章

@wuu

2015年学术文章

@zh

2015年学术文章

@zh-cn

2015年学术文章

@zh-hans

2015年学术文章

@zh-my

2015年学术文章

@zh-sg

2015年學術文章

@yue

2015年學術文章

@zh-hant

name

Highly enantioselective asymmetric transfer hydrogenation (ATH) of α-phthalimide ketones.

@en

Highly enantioselective asymmetric transfer hydrogenation

@nl

type

Item

label

Highly enantioselective asymmetric transfer hydrogenation (ATH) of α-phthalimide ketones.

@en

Highly enantioselective asymmetric transfer hydrogenation

@nl

prefLabel

Highly enantioselective asymmetric transfer hydrogenation (ATH) of α-phthalimide ketones.

@en

Highly enantioselective asymmetric transfer hydrogenation

@nl

P1476

Highly enantioselective asymmetric transfer hydrogenation (ATH) of α-phthalimide ketones.

@en

P2093

Jing Liu

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

Ke Li

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

Nan Wu

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

Rongli Zhang

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

Songlei Zhu

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

Yi Liu

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

Yong Li

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

Zhou Xu

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

P2860

Highly enantioselective ruthenium-catalyzed reduction of ketones employing readily available Peptide ligands.

Asymmetric transfer hydrogenation of ketones with bifunctional transition metal-based molecular catalysts.

Asymmetric transfer hydrogenation: chiral ligands and applications.

Mechanistic aspects of transition metal-catalyzed hydrogen transfer reactions.

Broader, greener, and more efficient: recent advances in asymmetric transfer hydrogenation.

Asymmetric hydrogenation, transfer hydrogenation and hydrosilylation of ketones catalyzed by iron complexes.

Asymmetric hydrogenation of ketones: tactics to achieve high reactivity, enantioselectivity, and wide scope.

Catalytic functionalization of tertiary alcohols to fully substituted carbon centres.

Highly enantioselective asymmetric hydrogenation of alpha-phthalimide ketone: an efficient entry to enantiomerically pure amino alcohols.

Asymmetric triple relay catalysis: enantioselective synthesis of spirocyclic indolines through a one-pot process featuring an asymmetric 6π electrocyclization.

P304

7513-7516

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

P31

scholarly article

P356

10.1039/C5OB00568J

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

P433

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

P478

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

P577

2015-07-01T00:00:00Z

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

P698

26068194

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

P921

enantioselectivity

Highly enantioselective asymmetric transfer hydrogenation (ATH) of α-phthalimide ketones.

about

P2860

P2860

Highly enantioselective asymmetric transfer hydrogenation (ATH) of α-phthalimide ketones.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921