A stereoselective route to 6-substituted pyrrolo-1,5-benzoxazepinones and their analogues

We developed a novel and convenient stereoselective path for the preparation of pyrrolo-1,5-benzoxazepinones (PBOs). This innovative route envisaged the employment of (−)-menthol as convenient chiral auxiliary and a key SNAr for the stereoselective preparation of a tertiary aryl–alkyl ether. As a fu...

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Veröffentlicht in:Tetrahedron letters 2013-09, Vol.54 (39), p.5387-5390
Hauptverfasser: Brindisi, Margherita, Gemma, Sandra, Alfano, Gloria, Kshirsagar, Giridhar, Novellino, Ettore, Campiani, Giuseppe, Butini, Stefania
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Sprache:eng
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Zusammenfassung:We developed a novel and convenient stereoselective path for the preparation of pyrrolo-1,5-benzoxazepinones (PBOs). This innovative route envisaged the employment of (−)-menthol as convenient chiral auxiliary and a key SNAr for the stereoselective preparation of a tertiary aryl–alkyl ether. As a further advancement, we exploited this newly conceived synthetic route for the preparation of 2-substituted PBO analogues to either undergo biological evaluation themselves or give access to a variety of further functionalization options.
ISSN:0040-4039
1873-3581
DOI:10.1016/j.tetlet.2013.07.115