The synthesis of orthogonally protected 3-(aminomethyl)-2-(carboxymethyl)isoxazolidinyl thymine, a convenient monomer for the preparation of novel isoxazolidinyl peptide nucleic acid analogues, has been achieved through enantioselective 1,3-dipolar cycloaddition between N-glycosyl nitrones and vinyl acetate.

3-(Aminomethyl)-2-(carboxymethyl)isoxazolidinyl nucleosides: building blocks for peptide nucleic acid analogues

CHIACCHIO, Ugo;CORSARO, Antonino;
2007

Abstract

The synthesis of orthogonally protected 3-(aminomethyl)-2-(carboxymethyl)isoxazolidinyl thymine, a convenient monomer for the preparation of novel isoxazolidinyl peptide nucleic acid analogues, has been achieved through enantioselective 1,3-dipolar cycloaddition between N-glycosyl nitrones and vinyl acetate.
ASYMMETRIC 1,3-DIPOLAR CYCLOADDITION; RESTRICTED PNA ANALOG; ENANTIOSELECTIVE SYNTHESIS
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/20.500.11769/35805
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