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
amides
diastereoselectivity
epoxides
regioselectivity
ring opening.
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/240457
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? 2
social impact