688044-83-9Relevant academic research and scientific papers
Synthesis of a 2,3-di-O-substituted heptose structure by regioselective 3-O-silylation of a 2-O-substituted heptose derivative
Ishii, Kazuyuki,Esumi, Yasuaki,Iwasaki, Youhei,Yamasaki, Ryohei
, p. 1214 - 1227 (2007/10/03)
A 3,4-diol derivative of 2-O-benzyl (Bn) heptose (Hep), methyl 6,7-di-O-acetyl-2-O-benzyl-L-glycero-α-D-manno-heptopyranoside (3), was treated with both triethylsilyl (TES) and tert-butyldimethylsilyl (TBDMS) chlorides to regioselectively form the 3-O-sil
