Borane-catalyzed metal-free hydrogenation of 2,7-disubstituted 1,8-naphthyridines.

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Borane-catalyzed metal-free hydrogenation of 2,7-disubstituted 1,8-naphthyridines.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

@wuu

2016年学术文章

@zh

2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

2016年學術文章

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name

Borane-catalyzed metal-free hydrogenation of 2,7-disubstituted 1,8-naphthyridines.

@en

Borane-catalyzed metal-free hydrogenation of 2,7-disubstituted 1,8-naphthyridines.

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label

Borane-catalyzed metal-free hydrogenation of 2,7-disubstituted 1,8-naphthyridines.

@en

Borane-catalyzed metal-free hydrogenation of 2,7-disubstituted 1,8-naphthyridines.

@nl

prefLabel

Borane-catalyzed metal-free hydrogenation of 2,7-disubstituted 1,8-naphthyridines.

@en

Borane-catalyzed metal-free hydrogenation of 2,7-disubstituted 1,8-naphthyridines.

@nl

P1476

Borane-catalyzed metal-free hydrogenation of 2,7-disubstituted 1,8-naphthyridines.

@en

P2093

Haifeng Du

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

Wei Wang

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

Xiangqing Feng

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

P2860

Indole naphthyridinones as inhibitors of bacterial enoyl-ACP reductases FabI and FabK

Reversible, metal-free hydrogen activation

Hydrogenations at room temperature and atmospheric pressure with mesoionic carbene-stabilized borenium catalysts.

2-Oxo-tetrahydro-1,8-naphthyridines as selective inhibitors of malarial protein farnesyltransferase and as anti-malarials

Frustrated Lewis pair chemistry: development and perspectives.

Frustrated Lewis Pairs.

Metal-free catalytic hydrogenation of polar substrates by frustrated Lewis pairs.

Nonpeptide alpha(v)beta(3) antagonists. 1. Transformation of a potent, integrin-selective alpha(IIb)beta(3) antagonist into a potent alpha(v)beta(3) antagonist.

Metal-free hydrogenation catalyzed by an air-stable borane: use of solvent as a frustrated Lewis base.

Enantioselective hydrogenation with chiral frustrated Lewis pairs.

P304

6683-6686

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P31

scholarly article

P356

10.1039/C6OB01172A

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

P433

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

P478

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

P577

2016-07-01T00:00:00Z

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

P698

27334098

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