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

✍ Scribed by W. Verboom; H.J. Berga; W.P. Trompenaars; D.N. Reinhoudt

Publisher: Elsevier Science
Year: 1985
Tongue: French
Weight: 299 KB
Volume: 26
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)89179-0

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✦ Synopsis

BenaeneacetonitriZes 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-, tetrahydropyridoCl,Z-a]indoZe or dihydro-l-benzazepin derivatives, respectively.

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