This submission belongs to the session a. General Organic Synthesis of the event The 9th International Electronic Conference on Synthetic Organic Chemistry
Published date
01 Nov, 2005
Citation
Alexander Balbuzano-Deus, Juan C. Rodríguez-Domínguez, Anais Fernández Villalobo, Miguel López-López, Gilbert Kirsch, Novel Synthesis of 6-chloroindoxyl-1,3-diacetate (Salmon), in Proceedings of The 9th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2005, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-9-01464
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Novel Synthesis of 6-chloroindoxyl-1,3-diacetate (Salmon)
Alexander Balbuzano-Deus 1
Juan C. Rodríguez-Domínguez 1
Anais Fernández Villalobo 1
Miguel López-López 1
Gilbert Kirsch 1
1. Departamento de Química, Centro de Química Farmacéutica, Calle 200 y 21, Atabey, Playa, CP 11600, Ciudad de la Habana, Cuba
Abstract
Nowadays the chromogenic substrates are very used for the quality control of different products such as water and food among others. These type of compounds are present as a component of some diagnostic media and allow to carry out the identification of different harmful bacteria. The enzimes excreted by the bacteries produce the lisis of the glycosidic linkage of the substrate showing a blue or magenta coloration [1]. One of these bacteria is the E. Coli that is identified by the 6-chloro-3-indolyl-b-D-glucuronide cyclohexylamine salt (Fig.1), among others[2,3], which present an indolic moiety as the aglycon part.
Keywords
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