157896-03-2Relevant articles and documents
AN EFFICIENT AND SCALABLE PROCESS FOR THE MANUFACTURE OF FONDAPARINUX SODIUM
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, (2013/08/15)
The present invention relates to a process for the synthesis of the Factor Xa anticoagulent Fondaparinux and related compounds. The invention relates, in addition, to efficient and scalable processes for the synthesis of various intermediates useful in the synthesis of Fondaparinux and related compounds.
A synthetic approach to aromatic aminoglycoside as a neamine mimic
Inoue, Ryo,Matsuda, Sho,Oda, Yoshiki,Ooyama, Hirofumi,Yoshida, Akihiro,Hamasaki, Keita,Yamanoi, Takashi
experimental part, p. 1335 - 1343 (2012/03/27)
This paper describes the synthetic approach to an aromatic a-glycoside as a mimic of neamine, which is a common core structure of some aminoglycoside antibiotics. We achieved the synthesis of the protected precursor of the neamine mimic, 4-(2,6-diamino-2,
Synthesis of disaccharidic sub-units of a new series of heparin related oligosaccharides
La Ferla, Barbara,Lay, Luigi,Guerrini, Marco,Poletti, Laura,Panza, Luigi,Russo, Giovanni
, p. 9867 - 9880 (2007/10/03)
The chemical synthesis of disaccharides 1 and 2, useful building-blocks for the preparation of a new series of heparin related oligosaccharides containing the unusual sequence (GlcN-IdoA)(n), is described. In addition, the orthogonality of the protective groups would allow access to a wide array of differently sulfated oligosaccharides. As the simplest members of this new class of oligomer, the synthesis of sulfated disaccharides 3 and 4 fully deprotected is reported.