Synthesis and 13C, 15N NMR study of a new functionalized pyrido[2,3-b]indole derivative

DOI: 10.1002/jhet.5570330368

Source and publish data:

Journal of Heterocyclic Chemistry p. 973 - 977 (1996)

Update date:2022-08-04

Topics:

Authors:

Buisson Buisson

Bisagni Bisagni

Monneret

Demerseman

Leon Leon

Platzer Platzer

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Article abstract of DOI:10.1002/jhet.5570330368

New functionalized α-carbolinones especially the 4-hydroxy-3-nitro-1H,9H-pyrido[2,3-b]indol-2-one were synthesized in a good yield, three-step reaction. A complete ¹³C, ¹⁵N nmr study of this carbolinone and precursors is presented.

Full text of DOI:10.1002/jhet.5570330368

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