The madelung synthesis of dihydro-1H-pyrrolo- and tetrahydropyrido[1,2-a]- indoles under mild conditions

Willem Verboom, H.J. Berga, W.P. Trompenaars, David Reinhoudt

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Abstract

Benzeneacetonitriles substituted with lactam moieties in the ortho-position cyclize under the influence of a base, dependent on the ring-size of the lactam function, to dihydropyrrolo-, tetrahydropyrido[1,2-a]indole or dihydro-1-benzazepin derivatives, respectively.
Original languageUndefined
Pages (from-to)685-688
JournalTetrahedron letters
Volume26
Issue number5
DOIs
Publication statusPublished - 1985

Keywords

  • IR-69436

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