Asymmetric 1,3-Dipolar Cycloadditons of Stabilized Azomethine Ylides with Nitroalkenes


Autoria(s): Nájera Domingo, Carmen; Sansano, Jose M.
Contribuinte(s)

Universidad de Alicante. Departamento de Química Orgánica

Universidad de Alicante. Instituto Universitario de Síntesis Orgánica

Síntesis Asimétrica (SINTAS)

Data(s)

05/06/2014

05/06/2014

2014

Resumo

This review highlights the biological importance of many polysubstituted nitro-prolines and -pyrrolidines. Their preparation using asymmetric 1,3-dipolar cycloadditions of azomethine ylides with nitroalkenes using diastereoselective and enantioselective strategies is described remarking the scope and main features of each one.

This work has been supported by the Spanish Ministerio de Economía y Competitividad (MINECO) (Consolider INGENIO 2010 CSD2007-00006, CTQ2010-20387), FEDER, Generalitat Valenciana (PROMETEO/2009/039), and by the University of Alicante.

Identificador

Current Topics in Medicinal Chemistry. 2014, 14(10): 1271-1282. doi:10.2174/1568026614666140423112145

1568-0266 (Print)

1873-5294 (Online)

http://hdl.handle.net/10045/37876

10.2174/1568026614666140423112145

Idioma(s)

eng

Publicador

Bentham Science Publishers

Relação

http://dx.doi.org/10.2174/1568026614666140423112145

Direitos

© 2014 Bentham Science Publishers

info:eu-repo/semantics/openAccess

Palavras-Chave #Antitumoral #Asymmetric synthesis #Catalysis #Cycloaddition #Metal #Organocatalyst #Química Orgánica
Tipo

info:eu-repo/semantics/article