Issue 5, 1996

Total synthesis of (±)-methylenolactocin by radical cyclisation of an epoxide using a transition-metal radical

Abstract

A stereoselective total synthesis of(±)-methylenotocin 1 is achieved via the radical cyclisation of an epoxide as a key step, using a titanium radical source.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1996, 403-404

Total synthesis of (±)-methylenolactocin by radical cyclisation of an epoxide using a transition-metal radical

G. Maiti and S. C. Roy, J. Chem. Soc., Perkin Trans. 1, 1996, 403 DOI: 10.1039/P19960000403

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