Oxidation of substituted 2-methylpyrroles with perhalogenated metalloporphyrins: A one-pot synthesis of dipyrromethanes

DOI: 10.1016/0040-4039(95)02231-7

Source and publish data:

Tetrahedron Letters p. 603 - 604 (1996)

Update date:2022-08-17

Topics:

Authors:

Karunaratne, Veranja

Dolphin, David

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Article abstract of DOI:10.1016/0040-4039(95)02231-7

A variety of substituted 2-methylpyrroles underwent allylic oxidation with the perchlorinated metalloporphyrin 2 and iodosylbenzene in TFA/CH₂Cl₂ (9:1). Subsequent addition of an α-free pyrrole to the same reaction mixture afforded a

Full text of DOI:10.1016/0040-4039(95)02231-7

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