The target compound was synthesized from N-benzyl protected aminoacetophenone through hydrogenation,benzoylation and reduction.
以氮-苄基保护胺基酮为原料,经,甲酰,还原三步合双甲酰沙丁胺醇酯。
The target compound was synthesized from N-benzyl protected aminoacetophenone through hydrogenation,benzoylation and reduction.
以氮-苄基保护胺基酮为原料,经,甲酰,还原三步合双甲酰沙丁胺醇酯。
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