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

Dentistry and Medical Sciences

Research output: Contribution to journal › Article › peer-review

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

Cite this

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

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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AU - Parkinson, Christopher J.

AU - Pinhey, John T.

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N2 - 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.

AB - 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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JO - Journal of the Chemical Society - Perkin Transactions 1

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IS - 5

ER -

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

Abstract

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