[Figure not available: see fulltext.] A convenient synthesis of 2- and/or 3-oxazolines has been developed depending on the structure and stereochemistry of the starting amino alcohol. PhI(OAc)2acted as oxidant on the intermediate imine, as supported by NMR investigation. The findings demonstrate a new route providing access to unusual 3-oxazolines.

Use of Hypervalent Iodine in the Synthesis of Isomeric Dihydrooxazoles

Carlucci, Claudia
Writing – Original Draft Preparation
;
2018-01-01

Abstract

[Figure not available: see fulltext.] A convenient synthesis of 2- and/or 3-oxazolines has been developed depending on the structure and stereochemistry of the starting amino alcohol. PhI(OAc)2acted as oxidant on the intermediate imine, as supported by NMR investigation. The findings demonstrate a new route providing access to unusual 3-oxazolines.
2018
Inglese
Inglese
54
4
428
436
9
http://www.springerlink.com/content/0009-3122
2-oxazolines
3-oxazolines
hypervalent iodine
NMR studies
stereoselective synthesis
Organic Chemistry
7
info:eu-repo/semantics/article
262
Carlucci, Claudia; Tota, Arianna; Colella, Marco; Ronamazzi, Giuseppe; Clarkson, Guy J.; Luisi, Renzo; Degennaro, Leonardo
1 Contributo su Rivista::1.1 Articolo in rivista
none
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14085/19937
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