Iminophosphorane-Mediated Synthesis of the Carbon Skeleton of the Azafluoranthene Alkaloids Rufescine and Imeluteine

1 January 1995

journal article
letter
Published by Georg Thieme Verlag KG in Synlett

Vol. 1995 (01) , 43-45
https://doi.org/10.1055/s-1995-4861

Abstract

A new four-step synthesis of the carbon skeleton of the azafluoranthene alkaloids rufescine and imeluteine based on a combitational aza Wittig/electrocyclic ring closure-intramolecular oxidative biaryl coupling is described.

Keywords

AZAFLUORANTHENE ALKALOIDS
AZA WITTIG/ELECTROCYCLIC RING-CLOSURE
OXIDATIVE BIARYL COUPLING
RUFESCINE
IMELUTEINE

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