作者:Takeyoshi Sugiyama、Tetsuya Murayama、Kyohei Yamashita、Takayuki Oritani
DOI:10.1271/bbb.59.1921
日期:1995.1
Aspyrone (1) was elaborated in an optically pure form by a key reaction involving the highly diastereoselective addition of tetrahydropyranone enol ate to 2-tosyloxy-aldehyde and the subsequent in situ formation of an epoxide.
Aspyrone(1)通过一项关键反应被精细制备成光学纯形式,该反应涉及高度立体选择性的四氢吡喃酮烯醇盐对2-对甲苯磺酰氧基醛的加成,随后在原位形成环氧乙烷。