Issue 7, 1990

Perkin communications. A new synthetic route to (±)-magydardienediol via a radical cyclisation-trapping reaction

Abstract

(±)-1 -epi-Magydardienediol, an intermediate for the synthesis of (±)-magydardienediol, has been synthesised stereoselectively from 3-methylcyclohex-2-enone in 12 steps via a sequential intra- and inter-molecular radical C–C bond-forming reaction.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1990, 2153-2154

Perkin communications. A new synthetic route to (±)-magydardienediol via a radical cyclisation-trapping reaction

H. Nagano, Y. Seko and K. Nakai, J. Chem. Soc., Perkin Trans. 1, 1990, 2153 DOI: 10.1039/P19900002153

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