716329-02-1Relevant articles and documents
An efficient synthesis of derivatives of 2-acetamido-4-amino-2,4,6- trideoxy-D-galactopyranose
Liang, Hong,Grindley
, p. 71 - 82 (2007/10/03)
Methyl 2-acetamido-4-amino-2,4,6-trideoxy-α-D-galactopyranoside (10) was synthesized from D-glucosamine hydrochloride in eight steps in an overall yield of 31%. Key steps include the selective benzoylation at O-3 of methyl 2-acetamido-2,6-dideoxy-α-D-glucopyranoside in 89% yield and the subsequent Mitsunobu reaction using diphenylphosphoryl azide as the azide source which proceeded in 92% yield. Di- and mono-benzyloxycarbonyl derivatives of 10 were also prepared. Copyright