A simple and efficient stereoselective synthesis of polysubstituted beta,gamma-epoxyhydroxylamines and 4-hydroxyalkyl-1,2-oxazetidines, based on the addition of alpha-lithiated aryloxiranes to nitrones and subsequent cyclization of the corresponding intermediates in a 4-exo-tet mode, is described.

Stereoselective Synthesis of Novel ?,?-Epoxyhydroxylamines and 4-Hydroxyalkyl-1,2-oxazetidines

Cuocci C
2006

Abstract

A simple and efficient stereoselective synthesis of polysubstituted beta,gamma-epoxyhydroxylamines and 4-hydroxyalkyl-1,2-oxazetidines, based on the addition of alpha-lithiated aryloxiranes to nitrones and subsequent cyclization of the corresponding intermediates in a 4-exo-tet mode, is described.
2006
Istituto di Cristallografia - IC
BETA-AMINO ACIDS; 1
3-DIPOLAR CYCLOADDITION REACTIONS; PROPARGYLIC N-HYDROXYLAMINES; KETENE-SILYL-ACETALS; TERMINAL ALKYNES; DIASTEREOSELECTIVE ADDITION; ORGANOMETALLIC REAGENTS; NUCLEOPHILIC ADDITIONS; ASYMMETRIC-SYNTHESIS; GRIGNARD ADDITION
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/13313
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