Aziridines from alkenyl-β-D-galactopyranoside derivatives: Stereoselective synthesis and in vitro selective anticancer activity-Reference-Cited by-同舟云学术

Aziridines from alkenyl-β-D-galactopyranoside derivatives: Stereoselective synthesis and in vitro selective anticancer activity

Published:2013-12 Issue: Volume:70 Page:380-392
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Vega-Pérez José M.,Palo-Nieto Carlos,Vega-Holm Margarita,Góngora-Vargas Purificación,Calderón-Montaño José Manuel,Burgos-Morón Estefanía,López-Lázaro Miguel,Iglesias-Guerra Fernando

Funder

Junta de Andalucía

Ministerio de Asuntos Exteriores y Cooperación

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference58 articles.

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2. Recent developments in regioselective ring opening of aziridines

3. Enantiomerically pure 2-aryl(alkyl)-2-trifluoromethylaziridines: synthesis and ring opening with selected O- and N-nucleophiles

4. Highly regio- and stereoselective ring-opening of epoxides and aziridines with sodium azide using ammonium-12-molybdophosphate

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