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Efficient synthesis of fully renewable, furfural-derived building blocks <i>via</i> formal Diels–Alder cycloaddition of atypical addends

Răzvan C. Cioc, Eva Harsevoort, Martin Lutz, Pieter C. A. Bruijnincx

2023Green Chemistry16 citationsDOIOpen Access PDF

Abstract

the furfural derivatives. Herein we describe the remarkably-facile intramolecular DA reaction of allyl acetals of different furfurals to efficiently afford formal DA adducts with the atypical, unreactive dienophile allyl alcohol. Our methodology gives access to unprecedented oxanorbornene derivatives in high chemo-, regio- and stereoselectivity, which can be readily diversified into valuable products. This offers the potential of scalable production of renewable chemical building blocks from cheap, bioderived platform molecules.

Topics & Concepts

CycloadditionFurfuralIntramolecular forceChemistryStereoselectivityAdductDiels–Alder reactionOrganic chemistryMoleculeCombinatorial chemistryCatalysisOxidative Organic Chemistry ReactionsSynthetic Organic Chemistry MethodsCatalytic Alkyne Reactions
Efficient synthesis of fully renewable, furfural-derived building blocks <i>via</i> formal Diels–Alder cycloaddition of atypical addends | Litcius