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Journal of Chemistry
Volume 2016 (2016), Article ID 2849140, 8 pages
http://dx.doi.org/10.1155/2016/2849140
Research Article

Reaction of Acyl Chlorides with In Situ Formed Zinc Selenolates: Synthesis of Selenoesters versus Ring-Opening Reaction of Tetrahydrofuran

1Group of Catalysis and Organic Green Chemistry, Department of Pharmaceutical Sciences, University of Perugia, Via del Liceo 1, 06100 Perugia, Italy
2Instituto de Química, Universidade Federal do Rio Grande do Sul (UFRGS), Avenida Bento Gonçalves 9500, 91501-970 Porto Alegre, RS, Brazil
3Laboratório de Síntese Orgânica Limpa (LASOL), Centro de Ciências Químicas, Farmacêuticas e de Alimentos (CCQFA), Universidade Federal de Pelotas (UFPel), P.O. Box 354, 96010-900 Pelotas, RS, Brazil

Received 2 March 2016; Accepted 24 May 2016

Academic Editor: Matthias D’hooghe

Copyright © 2016 Gemma Bellino et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

Gemma Bellino, Marialaura Scisciani, Jaqueline Pinto Vargas, et al., “Reaction of Acyl Chlorides with In Situ Formed Zinc Selenolates: Synthesis of Selenoesters versus Ring-Opening Reaction of Tetrahydrofuran,” Journal of Chemistry, vol. 2016, Article ID 2849140, 8 pages, 2016. doi:10.1155/2016/2849140