【摘 要】
:
1-epi-Castanospermine(5) was synthesized from readily available 2,3,4,6-tetra-O-benzyl-1-deoxynojirimycin(11) in 9 steps and 21% overall yield, with selective d
【机 构】
:
Beijing National Laboratory for Molecular Science(BNLMS), CAS Key Laboratory of Molecular Recognitio
【出 处】
:
Chinese Chemical Letters
论文部分内容阅读
1-epi-Castanospermine(5) was synthesized from readily available 2,3,4,6-tetra-O-benzyl-1-deoxynojirimycin(11) in 9 steps and 21% overall yield, with selective debenzylation, Barbier reaction and reductive amination as the main reaction steps.
1-epi-Castanospermine (5) was synthesized from readily available 2,3,4,6-tetra-O-benzyl-1-deoxynojirimycin (11) in 9 steps and 21% overall yield, with selective debenzylation, Barbier reaction and reductive amination as the main reaction steps.
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