An efficient and operationally simple method for the synthesis of functionalized azaoxobicyclo[X.3.0]alkane amino acids has been devised. The key step is an intramolecular nitrone cycloaddition on 5-allyl- or 5-homoallylproline that was found to be completely regio- and stereoselective.

Functionalised azabicycloalkane amino acids by nitrone 1,3-dipolar intramolecular cycloaddition

L Manzoni;D Arosio;
2005

Abstract

An efficient and operationally simple method for the synthesis of functionalized azaoxobicyclo[X.3.0]alkane amino acids has been devised. The key step is an intramolecular nitrone cycloaddition on 5-allyl- or 5-homoallylproline that was found to be completely regio- and stereoselective.
2005
Istituto di Scienze e Tecnologie Molecolari - ISTM - Sede Milano
INDUCER DIPEPTIDE MIMICS
BETA-TURN MIMETICS
SECONDARY STRUCTURE MIMETICS
PEPTIDE BACKBONE GEOMETRY
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/75561
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