作者:David R Tortolani、Scott A Biller
DOI:10.1016/0040-4039(96)01222-1
日期:1996.8
A procedure for the preparation of various analogs of miconazole on solid support is described. A novel iodoetherification transformation is utilized as the key synthetic step. This approach has been applied to the combinatorial synthesis of 45 analogs.
描述了在固体载体上制备咪康唑的各种类似物的方法。一种新型的碘醚化转化被用作关键的合成步骤。此方法已应用于45种类似物的组合合成。