Accessing polysubstituted oxazolidines, pyrrolidines and imidazolidines by regioselective [3 + 2] annulations of ketenimines with donor–acceptor oxiranes and aziridines-Reference-Cited by-同舟云学术

Accessing polysubstituted oxazolidines, pyrrolidines and imidazolidines by regioselective [3 + 2] annulations of ketenimines with donor–acceptor oxiranes and aziridines

Published:2018 Issue:13 Volume:5 Page:2020-2029
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Alajarin Mateo¹²³⁴⁵^ORCID,Bañon Daniel¹²³⁴⁵,Egea Adrian¹²³⁴⁵,Marín-Luna Marta¹⁶⁷⁸^ORCID,Orenes Raul-Angel⁹²⁴¹⁰⁸,Vidal Angel¹²³⁴⁵^ORCID

Affiliation:

1. Departamento de Química Orgánica

2. Universidad de Murcia

3. Facultad de Química

4. Regional Campus of International Excellence “Campus Mare Nostrum”

5. 30100 Murcia

6. Universidad de Vigo

7. Vigo

8. Spain

9. Servicio Universitario de Instrumentación Científica

10. Murcia

Abstract

Diverse five-membered rings result from formal [3 + 2] cycloadditions of ketenimines with carbonyl and azomethine ylides.

Funder

Ministerio de Economía y Competitividad

Fundación Séneca

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/QO/C8QO00255J

Reference100 articles.

1. Asymmetric 1,3-Dipolar Cycloaddition Reactions

2. Organotransition metal [3+2] cycloaddition reactions

3. Metal-Assisted Stereocontrol of 1,3-Dipolar Cycloaddition Reactions

4. Construction of Enantiopure Pyrrolidine Ring System via Asymmetric [3+2]-Cycloaddition of Azomethine Ylides

5. Intramolecular 1,3-dipolar cycloaddition reactions in targeted syntheses

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