Diversity-oriented synthesis of dihydrobenzoxazepinones by coupling the Ugi multicomponent reaction with a Mitsunobu cyclization
2014 ◽
Vol 10
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pp. 209-212
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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)benzylamines have been in situ generated from the corresponding azides, in turn prepared in high yields from salicylic derivatives.
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2016 ◽
Vol 40
(12)
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pp. 10300-10304
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2015 ◽
Vol 93
(5)
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pp. 542-545
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2019 ◽
Vol 17
(41)
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pp. 9217-9225
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2012 ◽
Vol 170-173
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pp. 1187-1191
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