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Tandem transformations of N-alkyl-N-allenylmethylanilines to N-alkyl-2-ethenylindoles

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TLDR
In this article, N-alkyl-N-allenylmethylanilines with magnesium monoperoxyphthalate in methanol-water underwent tandem transformations to furnish Nalkyl 2-ethenylindoles in good yield.
Abstract
Treatment of N-alkyl-N-allenylmethylanilines with magnesium monoperoxyphthalate in methanol–water underwent tandem transformations to furnish N-alkyl-2-ethenylindoles in good yield.

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Journal ArticleDOI

Tandem Transformations of N‐Alkyl‐N‐allenylmethylanilines to N‐Alkyl‐2‐ ethenylindoles.

TL;DR: In this article, N-alkyl-N-allenylmethylanilines with magnesium monoperoxyphthalate in methanol-water underwent tandem transformations to furnish Nalkyl 2-ethenylindoles in good yield.
References
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Journal ArticleDOI

Synthesis of carbazole alkaloids

TL;DR: An account of the authors work on the synthesis of carbazole alkaloids is presented in this article, along with relevant work from other groups as well as a review of hyellazoles and carbazomycins.
Journal ArticleDOI

Hetero-cope rearrangements - vI1 short and stereoselective syntheses of 2-vinylindoles by a tandem-process

TL;DR: In this article, the initially formed N-phenylnitrone-intermediates are converted by a tandem reaction (cycloaddition, Cope rearrangement, retro-Michael addition, and indolization) to 2-vinylindoles.
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