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Diversity-oriented synthesis of dihydrobenzoxazepinones by coupling the Ugi multicomponent reaction with a Mitsunobu cyclization

An operationally simple protocol for the synthesis of 2,3-dihydrobenzo[f][1,4]oxazepin-3-ones, based on an Ugi reaction of an ortho-(benzyloxy)benzylamine, glycolic acid, an isocyanide and an aldehyde, followed by an intramolecular Mitsunobu substitution was developed. The required ortho-(benzyloxy)...

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Bibliografische gegevens
Hoofdauteurs: Lisa Moni, Luca Banfi, Andrea Basso, Alice Brambilla, Renata Riva
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Beilstein-Institut 2014-01-01
Reeks:Beilstein Journal of Organic Chemistry
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Online toegang:https://doi.org/10.3762/bjoc.10.16
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