An unprecedented one-pot reaction that allows the synthesis of diprotected amino alcohols from unprotected vinyl aziridines is reported. The results demonstrate the possibility to use various acyl chlorides in order to obtain differently functionalised fragments. Mechanistic insights are given. (C) 2013 Elsevier Ltd. All rights reserved.

New one-pot procedure for the synthesis of diprotected amino alcohols from unprotected vinyl aziridines

Righi Giuliana;Bovicelli Paolo;
2013

Abstract

An unprecedented one-pot reaction that allows the synthesis of diprotected amino alcohols from unprotected vinyl aziridines is reported. The results demonstrate the possibility to use various acyl chlorides in order to obtain differently functionalised fragments. Mechanistic insights are given. (C) 2013 Elsevier Ltd. All rights reserved.
2013
Istituto di Chimica Biomolecolare - ICB - Sede Pozzuoli
STEREOSELECTIVE-SYNTHESIS
7-MEMBERED LACTAMS
VINYLAZIRIDINES
ISOMERIZATION
REARRANGEMENT
AZIDOLYSIS
ISOSTERES
ANALOGS
ESTERS
ROUTE
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/250061
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