132183-14-3Relevant academic research and scientific papers
A highly stereoselective synthesis of di- and trimeric sialosyltn epitope: A partial structure of glycophorin A
Nakahara, Yoshiaki,Iijima, Hiroyuki,Sibayama, Shohei,Ogawa, Tomoya
, p. 6897 - 6900 (1990)
Di- and trimeric sialosyl-Tn epitope, prototype molecules of O-linked (mucin type) sialoglycoproteins, were synthesized in a stereocontrolled manner.
One-Step TEMPO-Catalyzed and Water-Mediated Stereoselective Conversion of Glycals into 2-Azido-2-deoxysugars with a PIFA-Trimethylsilyl Azide Reagent System
Chennaiah, Ande,Vankar, Yashwant D.
supporting information, p. 2611 - 2614 (2018/05/17)
An unprecedented water-mediated and TEMPO-catalyzed, one-step, highly regiospecific and stereoselective functionalization of glycals to 2-azido-2-deoxysugars has been developed using a PIFA-Me3SiN3 reagent system in the presence of B
Synthesis of Tunicaminyluracil Derivatives
Ichikawa, Satoshi,Matsuda, Akira
, p. 239 - 253 (2007/10/03)
A tunicaminyluracil derivative, which is a key component of the tunicamycin nucleoside antibiotics, was synthesized using a samarium diiodide (Sml2) mediated aldol reaction and intramolecular Pummerer reaction as the key steps. The α-phenylthio
Stereoselective total synthesis of glycopeptides bearing the dimeric and trimeric sialosyl-Tn epitope
Nakahara, Yoshiaki,Iijima, Hiroyuki,Shibayama, Shohei,Ogawa, Tomoya
, p. 211 - 225 (2007/10/02)
The dimeric and trimeric sialosyl-Tn epitopes, 6)-α-D-GalpNAc-(1->3)-L-Ser>n-L-Val (n = 2 and 3), which represent part of a clustered carbohydrate region of glycophorin A, a human erythrocyte glycoprotein, have been synthesised
