作者:Gerald Dyker、Daniel Kadzimirsz、Andreas Thöne
DOI:10.1002/ejoc.200300216
日期:2003.8
The synthesis of the important carcinogens 1-nitrobenzo[a]pyrene and 3-nitrobenzo[a]pyrene was achieved in four steps starting from the parent compound. A hexyl ester functionality was introduced as a removable blocking group, controlling the regioselectivity of the synthesis. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)
重要致癌物 1-硝基苯并 [a] 芘和 3-硝基苯并 [a] 芘的合成从母体化合物开始,分四步完成。引入己酯官能团作为可去除的保护基团,控制合成的区域选择性。(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)