Experimental and computational investigation of the unexpected formation of β-substituted polyoxygenated furans from conveniently functionalized carbohydrates

In the course of our current studies on the reactivity of alkylidenecarbenes, prepared with the trimethylsilylazide/Bu2SnO method, on conveniently functionalized α-cyanomesylates derived from d-allose, d-arabinose, and d-threose, we have observed the unexpected, but mechanistically interesting formation of enantiomerically β-substituted polyhydroxylated furans. These compounds are the result of a series of cascade fragmentation reactions on unstable intermediates obtained during 1,5C-H insertion reactions from alkylidenecarbenes. The mechanism of the reaction has been investigated by computational methods using DFT analysis.

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