Issue 3, 1999

The synthesis of some 6,7-annulated codeines

Abstract

A benzofuro[6,7-b]morphinan related to naltriben has been synthesised using a radical induced cyclisation of 6β-O-(2-bromophenyl)codeine, itself prepared by a Mitsunobu reaction between codeine and 2-bromophenol. A Stille coupling between codeine 6-O-trifluoromethanesulfonate and vinyltri(butyl)tin leads to a 6-deoxyvinyl-codeine derivative, which can be reacted with electron-poor dienophiles to afford 6,7-fused cycloadducts.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1999, 241-244

The synthesis of some 6,7-annulated codeines

M. Liu, M. Sainsbury and N. Carter, J. Chem. Soc., Perkin Trans. 1, 1999, 241 DOI: 10.1039/A809701A

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