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- W2949492092 abstract "A straightforward synthesis of fully substituted β-carbolines via Brønsted acid promoted cyclizations of α-indolyl propargylic alcohols with nitrones is described. The use of nitrones bearing alkenyl or electron-rich aryl groups as the R4 substituent dramatically switches the reaction pathway to afford tetrasubstituted alkenes and amines, which is assumed to proceed through a rearrangement reaction involving N–O bond cleavage and 1,2-migration of the R4 group to an adjacent nitrogen atom." @default.
- W2949492092 created "2019-06-27" @default.
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- W2949492092 date "2012-11-12" @default.
- W2949492092 modified "2023-09-23" @default.
- W2949492092 title "Facile Synthesis of Fully Substituted Dihydro-β-carbolines via Brønsted Acid Promoted Cascade Reactions of α-Indolyl Propargylic Alcohols with Nitrones" @default.
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- W2949492092 doi "https://doi.org/10.1021/ol302695p" @default.
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