1327280-57-8Relevant articles and documents
Protecting group free synthesis of urea-linked glycoconjugates: Efficient synthesis of β-urea glycosides in aqueous solution
Ichikawa, Yoshiyasu,Minami, Takahiro,Kusaba, Shohei,Saeki, Nobuyoshi,Tonegawa, Yuta,Tomita, Yumiko,Nakano, Keiji,Kotsuki, Hiyoshizo,Masuda, Toshiya
supporting information, p. 3924 - 3931 (2014/06/09)
A method for the protecting group free synthesis of β-urea-linked glycoconjugates has been developed. The one step process, involving reactions between urea and d-glucose, N-acetyl-d-glucosamine or d-xylose in acidic aqueous solution, furnishes the corresponding β-urea glycosides in modest yields. This simple and efficient procedure is applicable to the synthesis of β-urea tethered amino acid-carbohydrate conjugates. This journal is the Partner Organisations 2014.