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Published on: February 9, 2021
Studies on the synthesis of furanosteroids. I. Viridin models
E Hampton Sessions1, Peter A Jacobi
1Department of Chemistry, Dartmouth College, Hanover, NH 03755, USA.
Abstract:
Alkyne oxazoles of general structure I are transformed directly to furo[2,3-b]phenol derivatives II by a sequence involving intramolecular Diels-Alder/retro-Diels-Alder reaction followed by tautomerization. Suitably functionalized phenols II undergo an intramolecular phenol-dienone-aldol condensation, generating the A,B,E-ring skeleton III characteristic of the viridin (1) class of furanosteroids.
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