Issue 9, 1993

Diastereoselective total syntheses of (±)-triptoquinone B and C

Abstract

The first and efficient total syntheses of (±)-triptoquinone B 1 and C 2 have been achieved from the allyl ether 3; the key steps are the construction of the four contiguous stereogenic centres present in 2 by the MnIII mediated oxidative free radical cyclisation followed by metal hydride reduction.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1993, 793-794

Diastereoselective total syntheses of (±)-triptoquinone B and C

K. Shishido, K. Goto, A. Tsuda, Y. Takaishi and M. Shibuya, J. Chem. Soc., Chem. Commun., 1993, 793 DOI: 10.1039/C39930000793

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