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- W2295176978 abstract "Abstract A novel and efficient route was established for the synthesis of a series of ( Z )-5-(2-(heteroaryl-2-yl) and ( Z )-5-(3-(heteroaryl-3-yl)-1-(phenyl)vinyl)-1 H -tetrazoles ( 3a – g and 6a – f , respectively) from cyanostilbene analogs containing benzo[ b ]thiophene, benzo[ b ]furan, and indole moieties utilizing tributyltin azide as a Lewis acid. This 1,3-dipolar [3+2]cycloaddition of azide to the cyano group of the cyanostilbene precursor molecule affords good yields of the corresponding tetrazolylstilbene analog and constitutes a simple and cost-effective procedure." @default.
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- W2295176978 date "2016-04-01" @default.
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- W2295176978 title "A novel and efficient tributyltin azide-mediated synthesis of 1H-tetrazolylstilbenes from cyanostilbenes" @default.
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- W2295176978 doi "https://doi.org/10.1016/j.tetlet.2016.03.040" @default.
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