New domino heteroannulation of enaminones: synthesis of diverse fused naphthyridines.

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Malononitrile dimer as a privileged reactant in design and skeletal diverse synthesis of heterocyclic motifs.A domino synthetic strategy leading to two-carbon-tethered fused acridine/indole pairs and fused acridine derivatives.

P2860

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P2860

New domino heteroannulation of enaminones: synthesis of diverse fused naphthyridines.

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http://www.wikidata.org/entity/Q50497858

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2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

@zh-cn

2012年学术文章

@zh-hans

2012年学术文章

@zh-my

2012年学术文章

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2012年學術文章

@yue

2012年學術文章

@zh-hant

name

New domino heteroannulation of enaminones: synthesis of diverse fused naphthyridines.

@en

New domino heteroannulation of enaminones: synthesis of diverse fused naphthyridines.

@nl

type

Item

label

New domino heteroannulation of enaminones: synthesis of diverse fused naphthyridines.

@en

New domino heteroannulation of enaminones: synthesis of diverse fused naphthyridines.

@nl

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New domino heteroannulation of enaminones: synthesis of diverse fused naphthyridines.

@en

New domino heteroannulation of enaminones: synthesis of diverse fused naphthyridines.

@nl

P1476

New domino heteroannulation of enaminones: synthesis of diverse fused naphthyridines.

@en

P2093

Bo Jiang

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

Jing Li

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

Man-Su Tu

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

Shu-Jiang Tu

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

Shu-Liang Wang

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

Yan Yu

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

P2860

Synthesis of 5,6,7,8-tetrahydro-1,6-naphthyridines and related heterocycles by cobalt-catalyzed [2 + 2 + 2] cyclizations.

Strategies for innovation in multicomponent reaction design.

Four-component domino reaction providing an easy access to multifunctionalized tricyclo[6.2.2.0(1,6)]dodecane derivatives.

Multicomponent reaction design in the quest for molecular complexity and diversity.

Multicomponent reactions for the synthesis of pyrroles.

Multicomponent reactions for the synthesis of heterocycles.

Multicomponent reactions and ionic liquids: a perfect synergy for eco-compatible heterocyclic synthesis.

Antiproliferative activity of novel benzo[b][1,6]naphthyridines in human solid tumor cell lines.

Pyridoacridine alkaloids inducing neuronal differentiation in a neuroblastoma cell line, from marine sponge Biemna fortis.

Synthesis of classical and nonclassical, partially restricted, linear, tricyclic 5-deaza antifolates.

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5361-5365

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scholarly article

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10.1039/C2OB25349F

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2012-04-30T00:00:00Z

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P698

22546930

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New domino heteroannulation of enaminones: synthesis of diverse fused naphthyridines.

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P2860

P2860

New domino heteroannulation of enaminones: synthesis of diverse fused naphthyridines.

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type

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698