Synlett 2015; 26(17): 2336-2350
DOI: 10.1055/s-0034-1378804
account
© Georg Thieme Verlag Stuttgart · New York

Diversity in Synthesis of N-Heterocycles from Simple Propargylic Alcohols

Eric Gayon
a   Institut Charles Gerhardt, UMR 5253 CNRS-UM2-UM1-ENSCM, 8 rue de l’École Normale, 34296 Montpellier Cedex 5, France   eMail: emmanuel.vrancken@enscm.fr   jean-marc.campagne@enscm.fr
,
Hélène Gerard
b   Laboratoire de Chimie Théorique, UMR 7616, UPMC—Université Paris 06, CNRS case 137, 4 Place Jussieu, 75262 Paris Cedex 05, France
,
Emmanuel Vrancken*
a   Institut Charles Gerhardt, UMR 5253 CNRS-UM2-UM1-ENSCM, 8 rue de l’École Normale, 34296 Montpellier Cedex 5, France   eMail: emmanuel.vrancken@enscm.fr   jean-marc.campagne@enscm.fr
,
Jean-Marc Campagne*
a   Institut Charles Gerhardt, UMR 5253 CNRS-UM2-UM1-ENSCM, 8 rue de l’École Normale, 34296 Montpellier Cedex 5, France   eMail: emmanuel.vrancken@enscm.fr   jean-marc.campagne@enscm.fr
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Publikationsverlauf

Received: 23. März 2015

Accepted after revision: 15. Juni 2015

Publikationsdatum:
01. September 2015 (online)


Abstract

In this account, we summarize our recent work on the preparation of various N-heterocycles, starting from propargylic alcohols. Our aim was to develop versatile and selective one-pot procedures that would permit the synthesis of large collections of heterocycles, such as di- or tri-substituted isoxazolines and isoxazoles, cis-aziridines, and pyrimidines, by fine changes in the reaction conditions. When needed, mechanistic studies have been performed by combining experimental work with density functional theory calculations.

1 Introduction

2 Synthesis of Disubstituted Isoxazolines

3 Synthesis of Disubstituted Isoxazoles

4 Synthesis of cis-Acylaziridines

5 Trisubstituted Isoxazolines and Isoxazoles

6 β-Enaminones and Pyrimidines

7 Conclusion