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
，
化，苯甲酰化，还原三步合成
苯甲酰沙丁胺醇酯。
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，化，苯甲酰化，还原三步合成苯甲酰沙丁胺醇酯。
声明：以
、词性分类均由互联网资源自动生成，部分未
过人工审核，其表达内容亦不代表本软件的观点；若发现问题，欢迎向我们指正。
