Anionic Cycloaddition Reactions Of Indole-2,3-dienolate With Dienophiles: A Facile Regiospecific Route To Substituted Carbazoles

DOI: 10.1016/0040-4039(95)00488-X

Source and publish data:

Tetrahedron Letters p. 3385 - 3388 (1995)

Update date:2022-08-30

Topics:

Authors:

Rao, Mandava V. Basaveswara

Satyanarayana, Janagani

Ila, Hiriyakkanavar

Junjappa, Hiriyakkanavar

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Article abstract of DOI:10.1016/0040-4039(95)00488-X

Indole 2,3-dienolate derived by deprotonation of 1,2-dimethylindole-3-carboxaldehyde is shown to be useful 1,4-dipole synthon (anionic indolo-2,3-quinodimethane) which undergoes facile cycloaddition with wide range of dienophiles affording substituted car

Full text of DOI:10.1016/0040-4039(95)00488-X

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