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

Verboom, W. and Berga, H.J. and Trompenaars, W.P. and Reinhoudt, D.N. (1985) The madelung synthesis of dihydro-1H-pyrrolo- and tetrahydropyrido[1,2-a]- indoles under mild conditions. Tetrahedron Letters, 26 (5). pp. 685-688. ISSN 0040-4039

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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.
Item Type:	Article
Copyright:	© 1985 Elsevier Science
Faculty:	Science and Technology (TNW)
Research Group:	Molecular Nanofabrication (MNF)
Link to this item:	http://purl.utwente.nl/publications/69436
Official URL:	http://dx.doi.org/10.1016/S0040-4039(00)89179-0
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