A new, mild and cheap aminolysis of 2,3-epoxy amides Ti(O-iPr)4 mediated has been developed. The reaction proceeds with excellent regioselectivity, regardless of the steric hindrance of the substituents on the heterocyclic ring, providing vicinal amino alcohols very suitable for synthetic applications.

Ti(O-iPr)4 promoted regio- and stereoselective aminolysis of 2,3-epoxy amides

Giuliana Righi;Lorenza Suber;
2012

Abstract

A new, mild and cheap aminolysis of 2,3-epoxy amides Ti(O-iPr)4 mediated has been developed. The reaction proceeds with excellent regioselectivity, regardless of the steric hindrance of the substituents on the heterocyclic ring, providing vicinal amino alcohols very suitable for synthetic applications.
2012
Istituto di Chimica Biomolecolare - ICB - Sede Pozzuoli
Istituto di Struttura della Materia - ISM - Sede Roma Tor Vergata
Inglese
13
1947
1949
3
Sì, ma tipo non specificato
amides
diastereoselectivity
epoxides
regioselectivity
ring opening.
2
info:eu-repo/semantics/article
262
Giuliana Righi; Agnese Mantineo; Lorenza Suber; Alessandra Mari
01 Contributo su Rivista::01.01 Articolo in rivista
none
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/240457
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