Iminophosphorane-mediated synthesis of functionalized indoles and 1,3-benzodiazepines

DOI: 10.1016/S0040-4039(00)92181-6

Source and publish data:

Tetrahedron Letters p. 4401 - 4404 (1991)

Update date:2022-07-30

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Authors:

Molina Molina

Arques Arques

Alias Alias

Vinader Vinader

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Article abstract of DOI:10.1016/S0040-4039(00)92181-6

Aza Wittig-type reaction of bis(iminophosphorane) 2 with aromatic isocyanates leads to either indoles 5 or pyrimido[4,5-b]indoles 6, whereas with aliphatic isocyanates and acyl chlorides afforded pyrrolo[2,3-b]indoles 7 and 1,3-benzodiazepines 10 respectively.

Full text of DOI:10.1016/S0040-4039(00)92181-6

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