A series of 9H-pyrrolo[1,2-a]indol-9-ones have been prepared via in-situ sequential oxidation of [2-(1Hpyrrol-1-yl)phenyl]methanols promoted by active manganese dioxide. The procedure led to title compoundsin good yields under mild conditions, without the need to isolate the intermediate aldehydes.

Efficient synthesis of 9H-pyrrolo[1,2-a]indol-9-one derivatives based on active manganese dioxide promoted intramolecular cyclization

AIELLO, Francesca;GAROFALO, Antonio
;
GRANDE, Fedora
2010

Abstract

A series of 9H-pyrrolo[1,2-a]indol-9-ones have been prepared via in-situ sequential oxidation of [2-(1Hpyrrol-1-yl)phenyl]methanols promoted by active manganese dioxide. The procedure led to title compoundsin good yields under mild conditions, without the need to isolate the intermediate aldehydes.
9H-Pyrrolo[1,2-a]indol-9-one
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11770/128633
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