Use of the electrophilic arylation reaction of aryllead triacetates in syntheses of (±)-O-methyljoubertiamine and (±)-mesembrine

Christopher J. Parkinson; John T. Pinhey

Use of the electrophilic arylation reaction of aryllead triacetates in syntheses of (±)-O-methyljoubertiamine and (±)-mesembrine

Christopher J. Parkinson, John T. Pinhey

Biomedical Sciences

Research output: Contribution to journal › Article

19 Citations (Scopus)

Abstract

p-Methoxyphenyllead triacetate and 3,4-dimethoxyphenyllead triacetate are used as electrophilic arylating agents to generate the quaternary benzylic centres in formal syntheses of (±)-O-methyljoubertiamine and (+)-mesembrine respectively.

Original language	English
Pages (from-to)	1053-1057
Number of pages	5
Journal	Journal of the Chemical Society, Perkin Transactions 1
Issue number	5
Publication status	Published - 1991

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Parkinson, C. J., & Pinhey, J. T. (1991). Use of the electrophilic arylation reaction of aryllead triacetates in syntheses of (±)-O-methyljoubertiamine and (±)-mesembrine. Journal of the Chemical Society, Perkin Transactions 1, (5), 1053-1057.

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abstract = "p-Methoxyphenyllead triacetate and 3,4-dimethoxyphenyllead triacetate are used as electrophilic arylating agents to generate the quaternary benzylic centres in formal syntheses of (±)-O-methyljoubertiamine and (+)-mesembrine respectively.",

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