PALLADIUM-CATALYZED, ONE-POT CARBONYLATION OF HETEROCYCLIC COMPOUNDS INTO THEIR ESTERS, IN THE PRESENCE OF MERCURY SALTS.

DOI: 10.1016/S0040-4039(00)87796-5

Source and publish data:

Tetrahedron Letters p. 6315 - 6318 (1986)

Update date:2022-08-05

Topics:

Authors:

Jaouhari, R.

Dixneuf, P. H.

Lecolier, S.

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Article abstract of DOI:10.1016/S0040-4039(00)87796-5

One pot carbonylation of tiophene, furan, benzofuran and pyrrole in alcohol, to produce the corresponding esters, has been carried out at room temperature, using a PdCl2/mercury salt/Copper(II) system.

Full text of DOI:10.1016/S0040-4039(00)87796-5

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