An efficient oxyfunctionalisation by dimethyldioxirane of the benzylethereal carbon of flavonoids; a general and useful way to anthocyanidins

DOI: 10.1016/S0040-4039(97)00958-1

Source and publish data:

Tetrahedron Letters p. 4651 - 4654 (1997)

Update date:2022-07-29

Topics:

Authors:

Bernini, Roberta

Mincione, Enrico

Sanetti, Anna

Bovicelli, Paolo

Lupattelli, Paolo

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Article abstract of DOI:10.1016/S0040-4039(97)00958-1

Compounds with flavonoid structure were selectively oxyfunctionalised at the C-2 carbon atom by DMD. The reaction permitted a new route to flavylium salts.

Full text of DOI:10.1016/S0040-4039(97)00958-1

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