Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction

dc.creatorStefani, Helio Alexandre
dc.creatorSilva, Nathalia C. S.
dc.creatorManarin, Flavia
dc.creatorLuedtke, Diogo S.
dc.creatorZukerman-Schpector, Julio
dc.creatorMadureira, Lucas Sousa
dc.creatorTiekink, Edward R. T.
dc.date.accessioned2013-10-25T14:12:31Z
dc.date.accessioned2018-07-04T16:02:20Z
dc.date.available2013-10-25T14:12:31Z
dc.date.available2018-07-04T16:02:20Z
dc.date.created2013-10-25T14:12:31Z
dc.date.issued2012
dc.identifierTETRAHEDRON LETTERS, OXFORD, v. 53, n. 14, p. 1742-1747, APR 4, 2012
dc.identifier0040-4039
dc.identifierhttp://www.producao.usp.br/handle/BDPI/36067
dc.identifier10.1016/j.tetlet.2012.01.102
dc.identifierhttp://dx.doi.org/10.1016/j.tetlet.2012.01.102
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1630782
dc.description.abstractWe have developed an efficient method for the synthesis of functionalized C-glycosyl 1,2,3-triazoles through a Cu(1)-promoted azide-alkyne 1,3-dipolar cycloaddition between a TMS-protected C-alkynyl-glycoside and organic azides. The reaction was accelerated by ultrasound irradiation and the addition of a base was not necessary to obtain the 1,2,3-triazole product. Moreover, further manipulation of the products led to chiral molecules with a C-glycoside linkage. (C) 2012 Elsevier Ltd. All rights reserved.
dc.languageeng
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD
dc.publisherOXFORD
dc.relationTETRAHEDRON LETTERS
dc.rightsCopyright PERGAMON-ELSEVIER SCIENCE LTD
dc.rightsclosedAccess
dc.subjectD-GLUCAL
dc.subject1,2,3-TRIAZOLE
dc.subjectCYCLOADDITION
dc.subjectCLICK CHEMISTRY
dc.subjectSELENOSUGARS
dc.titleSynthesis of 1,2,3-triazolylpyranosides through click chemistry reaction
dc.typeArtículos de revistas


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