Simple synthesis of furanoid and dioxabicyclo[3.3.0]octane lignans

Abstract
The key intermediates, the keto lactones 5, 6 obtained by convergent synthesis, were transformed into furanoid and dioxabicyclo[3.3.0]octane lignan analogues 7, 8 by means of sodium borohydride reduction and subsequent acid-catalysed cyclisation.

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