作者:Hisao Ona、Shoichiro Uyeo
DOI:10.1016/s0040-4039(01)80220-3
日期:1984.1
Total synthesis of dl-asparenomycins was accomplished with direct conversion of carbonates 13a, 13b and 14a, 14b to asparenomycin esters 15 and 16 and carboxy deprotection by the AlCl3-anisole method.
通过将
碳酸盐13a,13b和14a,14b直接转化为天冬
酰胺酯15和16并通过AlCl 3-
茴香醚方法使羧基
脱保护,从而完成dl-
阿斯巴霉素的全合成。