Synthesis of amino ester-embedded benzimidazoles: a one-pot sequential protocol under metal-free neutral conditions.

about

Synthesis of amino ester-embedded benzimidazoles: a one-pot sequential protocol under metal-free neutral conditions.

Item

http://www.wikidata.org/entity/Q53569965

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

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

@zh-hant

name

Synthesis of amino ester-embed ...... metal-free neutral conditions.

@en

Synthesis of amino ester-embed ...... metal-free neutral conditions.

@nl

type

Item

label

Synthesis of amino ester-embed ...... metal-free neutral conditions.

@en

Synthesis of amino ester-embed ...... metal-free neutral conditions.

@nl

prefLabel

Synthesis of amino ester-embed ...... metal-free neutral conditions.

@en

Synthesis of amino ester-embed ...... metal-free neutral conditions.

@nl

P1476

Synthesis of amino ester-embed ...... metal-free neutral conditions.

@en

P2093

Animesh Pramanik

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

Chandan Bodhak

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

Priyabrata Roy

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

P2860

Copper-catalyzed, one-pot, three-component synthesis of benzimidazoles by condensation and C-N bond formation

An experimental and computational analysis on the differential role of the positional isomers of symmetric bis-2-(pyridyl)-1H-benzimidazoles as DNA binding agents.

Synthesis and Anti-inflammatory Evaluation of Novel Benzimidazole and Imidazopyridine Derivatives

Copper-catalyzed intramolecular C-N bond formation: a straightforward synthesis of benzimidazole derivatives in water.

Pharmacokinetics of an emerging new class of anticoagulant/antithrombotic drugs. A review of small-molecule thrombin inhibitors.

The combinatorial synthesis of bicyclic privileged structures or privileged substructures.

Synthesis and biological activity evaluation of 1H-benzimidazoles via mammalian DNA topoisomerase I and cytostaticity assays.

Antimicrobial activity and a SAR study of some novel benzimidazole derivatives bearing hydrazone moiety.

Design, synthesis, SAR, and biological evaluation of highly potent benzimidazole-spaced phosphono-alpha-amino acid competitive NMDA antagonists of the AP-6 type.

Potential anxiolytic agents. Part 4: novel orally-active N(5)-substituted pyrido[1,2-a]benzimidazoles with high GABA-A receptor affinity.

P2888

s11030-016-9701-z

P304

89-100

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

P31

scholarly article

P356

10.1007/S11030-016-9701-Z

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

P433

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

P478

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

P577

2016-09-27T00:00:00Z

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

P698

27677738

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