Synthesis and biological evaluation of n
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Susana M. M. Lopes; Mafalda Laranjo; ArmΓ©nio C. Serra; Ana Margarida Abrantes; A
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Article
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2010
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Journal of Heterocyclic Chemistry
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English
β 479 KB
## Abstract magnified image Naphthoquinones undergo 1,3βdipolar cycloaddition with bicyclic mΓΌnchnones generated from thiazolidines affording new pyrroloβthiazoles with a fused quinone nucleus. The products were obtained as single enantiomers in good yields. These benzo[__f__]thiazolo[4,3β__a__]iso