作者:Tsuyoshi Ogiku、Masahiko Seki、Masami Takahashi、Hiroshi Ohmizu、Tameo Iwasaki
DOI:10.1016/s0040-4039(00)97879-1
日期:1990.1
1-Arylnaphthalene lignans were synthesized in good yields from O-t-butyldimethylsilylcyanohydrins in two steps based on a new approach involving a tandem conjugate addition-aldol reaction, followed by an acid-catalyzed construction of the naphthalene ring.
基于涉及串联共轭加成-醛醇缩合反应的新方法,然后通过酸催化的萘环的构建,由O-叔丁基二甲基甲硅烷基氰醇分两步以高收率合成了1-芳基萘木酚素。