Canthine analogs via intramolecular Diels-Alder reactions

DOI: 10.1016/0040-4020(95)00925-6

Source and publish data:

Tetrahedron p. 461 - 470 (1996)

Update date:2022-08-11

Topics:

Authors:

Markgraf, J. Hodge

Finkelstein, Manuel

Cort, John R.

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Article abstract of DOI:10.1016/0040-4020(95)00925-6

Carbocyclic analogs (10 and 12) of canthine (1) and canthin-6-one (2) were prepared in three and four steps, respectively, from indole-3-carboxyaldehyde. The key step was an intramolecular Diels-Alder reaction carried out in refluxing sulfolane.

Full text of DOI:10.1016/0040-4020(95)00925-6

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