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Triazolbenzo[d]thiazoles: efficient synthesis and biological evaluation as neuroprotective agents.


ABSTRACT: A number of (1H-1,2,3-triazol-1-yl)benzo[d]thiazoles were synthesized utilizing a versatile Cu-catalyzed azide-alkyne click reaction (CuAAC) on tautomeric benzo[4,5]thiazolo[3,2-d]tetrazole (1) and 2-azidobenzo[d]thiazole (2) starting materials. Moreover, one of the resulting products of this investigation, triazolbenzo[d]thiazole 22, was found to possess significant neuroprotective activity in human neuroblastoma (SH-SY5Y) cells.

SUBMITTER: Avila B 

PROVIDER: S-EPMC3432163 | biostudies-literature | 2012 Sep

REPOSITORIES: biostudies-literature

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Triazolbenzo[d]thiazoles: efficient synthesis and biological evaluation as neuroprotective agents.

Avila Belem B   Roth Aaron A   Streets Heather H   Dwyer Donard S DS   Kurth Mark J MJ  

Bioorganic & medicinal chemistry letters 20120720 18


A number of (1H-1,2,3-triazol-1-yl)benzo[d]thiazoles were synthesized utilizing a versatile Cu-catalyzed azide-alkyne click reaction (CuAAC) on tautomeric benzo[4,5]thiazolo[3,2-d]tetrazole (1) and 2-azidobenzo[d]thiazole (2) starting materials. Moreover, one of the resulting products of this investigation, triazolbenzo[d]thiazole 22, was found to possess significant neuroprotective activity in human neuroblastoma (SH-SY5Y) cells. ...[more]

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