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- W2908938870 endingPage "887" @default.
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- W2908938870 abstract "A Suzuki-Miyaura cross coupling, followed by triphenylphosphine mediated Cadogan reductive cyclization sequence provided efficient access to a series of carbazole alkaloids. In the present work, this approach was applied to the total synthesis of mukonine, clauszoline K, koenoline, murrayanine, murrayafoline A, mukoeic acid, glycoborine, glycozolicine, mukolidine, mukoline, glycozoline, 3-methoxy-9H-carbazole-1-carboxylic acid methyl ester, (3-methoxy-9H-carbazol-1-yl)-methanol, 3-methoxy-9H-carbazole-1-carbaldehyde, 3-methoxy-9H-carbazole-1-carboxylic acid, 2-methyl-9H-carbazole and nonsteroidal anti-inflammatory drug (NSAID) carprofen and its derivatives." @default.
- W2908938870 created "2019-01-25" @default.
- W2908938870 creator A5001791741 @default.
- W2908938870 creator A5021173408 @default.
- W2908938870 creator A5058031388 @default.
- W2908938870 creator A5058162191 @default.
- W2908938870 date "2019-02-01" @default.
- W2908938870 modified "2023-09-26" @default.
- W2908938870 title "Total synthesis of carbazole alkaloids" @default.
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- W2908938870 doi "https://doi.org/10.1016/j.tet.2019.01.003" @default.
- W2908938870 hasPublicationYear "2019" @default.
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