作者:A.J Poss、R.K Belter
DOI:10.1016/s0040-4039(00)96146-x
日期:1987.1
The synthesis of delesserine, 1, leucodrin, 2, and dilaspirolactone aglycone, 3, are reported. The preparation of these ascorbigens was implemented by the addition of ascorbic acid to a -hydroxy benzyl alcohol derived quinone methide.
据报道,合成了1,2,2,2,3,4,4,4,4,4,4,4,4,4,4,4,8,8,8,8,8,8,8,8,8,8,8,8,3,4,3,4,3,4,3,4,3,4,3,3,4,8,8,8,8,8,7,8。。。。。。。。。。。。。。。。。。。。。。。。。。.。。。。。。。。。。。。。。。。。。。。。。。。。类一家)。这些抗坏血酸的制备是通过将抗坏血酸添加到-羟基苯甲醇衍生的醌甲基化物中来实现的。