Two monomers for the syntheses of conformationally restricted peptide nucleic acids were synthesized through a simple procedure, involving an asymmetric 1,3-dipolar cycloaddition chemistry as a key step, from common starting materials in 3 and 5 steps, and 58.8% and 30.5% overall yields, respectively.

High-yield synthesis of pyrrolidinyl PNA monomers

CHIACCHIO, Ugo;CORSARO, Antonino;PISTARA', Venerando;
2011-01-01

Abstract

Two monomers for the syntheses of conformationally restricted peptide nucleic acids were synthesized through a simple procedure, involving an asymmetric 1,3-dipolar cycloaddition chemistry as a key step, from common starting materials in 3 and 5 steps, and 58.8% and 30.5% overall yields, respectively.
2011
Pyrrolidines; Nitrones; Nucleoside analogues; Peptide nucleic acids ; Dipolar cycloaddition
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11769/8529
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