905267-00-7Relevant academic research and scientific papers
Sub-stoichiometric reductive etherification of carbohydrate substrates and one-pot protecting group manipulation
Chen, Chiao Wen,Li, Xin Ru,Mong, Kwok-Kong Tony,Wang, Ching Chi,Witek, Henryk
supporting information, p. 3135 - 3141 (2020/05/08)
In this study, we report a new reductive etherification procedure for protection of carbohydrate substrates and its application for one-pot preparation of glycosyl building blocks. The reported procedure features the use of polymethylhydrosiloxane (PMHS)
SIALIDASE-RESISTANT SACCHARIDE AND METHOD OF MAKING AND USING THE SAME
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Page/Page column 13; 30-31, (2020/10/20)
Disclosed are a method of preparing a saccharide that contains a 3-fluoro-sialic acid and a method of bonding it to a homogeneous antibody. Also within the scope of this invention are compounds each containing a 3-fluoro-sialic acid, monoclonal antibodies bonded to α2,6-linked 3-fluoro-sialoside terminated N-glycans, and treatment of cancer with such monoclonal antibodies.
Towards glucosamine building blocks: Regioselective one-pot protection and deallylation procedures
Enugala, Ramu,Carvalho, Luísa C. R.,Marques, M. Manuel B.
scheme or table, p. 2711 - 2716 (2011/02/16)
Glucosamine building blocks have been prepared by an efficient regioselective one-pot protection approach. This synthetic route enabled the straightforward preparation of a glucosamine disaccharide in 73% yield. The system Pd(PPh3)4/
Iterative one-pot syntheses of chitotetroses
Huang, Lijun,Wang, Zhen,Li, Xiaoning,Ye, Xin-shan,Huang, Xuefei
, p. 1669 - 1679 (2007/10/03)
Rapid syntheses of chitotetrose derivatives were achieved in good yields using the newly developed reactivity independent iterative one-pot strategy. The protective groups on donors and acceptors were independently evaluated allowing matching of the two p
