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Synlett 1995; 1995(1): 43-45
DOI: 10.1055/s-1995-4861
DOI: 10.1055/s-1995-4861
letter
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Iminophosphorane-Mediated Synthesis of the Carbon Skeleton of the Azafluoranthene Alkaloids Rufescine and Imeluteine
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Publikationsverlauf
Publikationsdatum:
31. Dezember 2000 (online)
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.
azafluoranthene alkaloids - aza Wittig/electrocyclic ring-closure - oxidative biaryl coupling - rufescine - imeluteine