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- W2950789462 endingPage "563" @default.
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- W2950789462 abstract "An efficient diversity-oriented synthetic approach to annulated 9H-benzo[b]pyrrolo[1,2-g][1,2,3]triazolo[1,5-d][1,4]diazepines has been developed using a Sc(OTf)3-catalyzed two-component tandem C-2 functionalization-intramolecular azide-alkyne 1,3-dipolar cycloaddition reaction. The reaction shows high substrate tolerance and provides a library of fused heterocycles that may lead to novel biologically active compounds or drug lead molecules." @default.
- W2950789462 created "2019-06-27" @default.
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- W2950789462 date "2013-12-18" @default.
- W2950789462 modified "2023-09-26" @default.
- W2950789462 title "Tandem C-2 Functionalization–Intramolecular Azide–Alkyne 1,3-Dipolar Cycloaddition Reaction: A Convenient Route to Highly Diversified 9<i>H</i>-Benzo[<i>b</i>]pyrrolo[1,2-<i>g</i>][1,2,3]triazolo[1,5-<i>d</i>][1,4]diazepines" @default.
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- W2950789462 doi "https://doi.org/10.1021/ol403420z" @default.
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