S8 -Mediated Cyclization of 2-Aminophenols/thiophenols with Arylmethyl Chloride: Approach to Benzoxazoles and Benzothiazoles.

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S8 -Mediated Cyclization of 2-Aminophenols/thiophenols with Arylmethyl Chloride: Approach to Benzoxazoles and Benzothiazoles.

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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

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2016年學術文章

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name

S8 -Mediated Cyclization of 2- ...... nzoxazoles and Benzothiazoles.

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S8 -Mediated Cyclization of 2- ...... nzoxazoles and Benzothiazoles.

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type

Item

label

S8 -Mediated Cyclization of 2- ...... nzoxazoles and Benzothiazoles.

@en

S8 -Mediated Cyclization of 2- ...... nzoxazoles and Benzothiazoles.

@nl

prefLabel

S8 -Mediated Cyclization of 2- ...... nzoxazoles and Benzothiazoles.

@en

S8 -Mediated Cyclization of 2- ...... nzoxazoles and Benzothiazoles.

@nl

P1476

S8 -Mediated Cyclization of 2- ...... nzoxazoles and Benzothiazoles.

@en

P2093

Dazhuang Miao

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Haifeng Gan

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

Qiang Pan

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

Renhe Hu

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

Shiqing Han

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

Xiaotong Li

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P2860

Biochemical and structural evaluation of highly selective 2-arylbenzoxazole-based transthyretin amyloidogenesis inhibitors

Difluoromethylbenzoxazole pyrimidine thioether derivatives: a novel class of potent non-nucleoside HIV-1 reverse transcriptase inhibitors

2-Pyridinone derivatives: a new class of nonnucleoside, HIV-1-specific reverse transcriptase inhibitors

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

Synthesis, metal ion binding, and biological evaluation of new anticancer 2-(2'-hydroxyphenyl)benzoxazole analogs of UK-1

2-Arylbenzothiazole as a privileged scaffold in drug discovery.

Transfer of sulfur: from simple to diverse.

Sulfur Containing Scaffolds in Drugs: Synthesis and Application in Medicinal Chemistry.

Synthesis and biological properties of benzothiazole, benzoxazole, and chromen-4-one analogues of the potent antitumor agent 2-(3,4-dimethoxyphenyl)-5-fluorobenzothiazole (PMX 610, NSC 721648).

Antitumor benzothiazoles. 26.(1) 2-(3,4-dimethoxyphenyl)-5-fluorobenzothiazole (GW 610, NSC 721648), a simple fluorinated 2-arylbenzothiazole, shows potent and selective inhibitory activity against lung, colon, and breast cancer cell lines.

P304

1770-1774

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scholarly article

P356

10.1002/ASIA.201600355

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P433

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P478

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P577

2016-04-28T00:00:00Z

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27124616

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