Synthesis of Mono-6-azidoß- Cyclodextrin Derivatives by Microwave Radiation

Journal Title: Journal of Pharmaceutical and Biomedical Sciences - Year 2017, Vol 7, Issue 4

Abstract

As everyone knows, natural cyclodextrin possesses many hydroxyl groups so that it is hard for selective modification of the cyclodextrin. In this research, we provide a new method to synthesize 1,2,3-1H-triazole-b-cyclodextrin derivatives so that we can settle the selective modification of the cyclodextrin. Meanwhile, we use microwave (MW) irradiation to perform the reaction instead of oil-bath heating, which is merciful to the environment. The 1,2,3-1H-triazole-b-cyclodextrin derivatives were synthesized by the MW irradiation reaction from mono-6-azido-b-CD with the yields of about 75%–88%. Their structures were characterized by 1H NMR, 13C NMR and ESI-MS.

Authors and Affiliations

Jiajing Guo, Jialiang Guo, Siyuchen . , Pinghua Sun

Keywords

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  • EP ID EP433723
  • DOI -
  • Views 110
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How To Cite

Jiajing Guo, Jialiang Guo, Siyuchen . , Pinghua Sun (2017). Synthesis of Mono-6-azidoß- Cyclodextrin Derivatives by Microwave Radiation. Journal of Pharmaceutical and Biomedical Sciences, 7(4), 100-102. https://europub.co.uk/articles/-A-433723