Iminophosphorane-mediated synthesis of 1-substituted-β-carbolines: Investigative studies on the preparation of alkaloids lavendamycin and eudistomins framework

DOI: 10.1016/S0040-4039(00)78888-5

Source and publish data:

Tetrahedron Letters p. 2891 - 2894 (1992)

Update date:2022-08-04

Topics:

Authors:

Molina, Pedro

Fresneda, Pilar M.

Canovas, Mercedes

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Article abstract of DOI:10.1016/S0040-4039(00)78888-5

Aza-Wittig reaction of iminophosphorane 3, derived from ethyl a-azido-β-(3-indolyl) propenoate and triphenylphosphine, with 2-formylpyrrole and 2-formylquinolines leads to Eudistomins A and M and Lavendamycin derivatives respectively.

Full text of DOI:10.1016/S0040-4039(00)78888-5

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