Synthesis, EPR, ENDOR and TRIPLE resonance investigations of anthracycline-related semiquinones
作者:Hartmut B. Stegmann、Thomas Jülich、Ulrike Höfler、Paul Schuler、Wolfhard Koch、Karsten Krohn、Astrid Eickhoff
DOI:10.1002/mrc.1260310510
日期:1993.5
substituted anthraquinones related to anthracyclines is described. One‐electron reduction of these compounds yields the corresponding semiquinones, which were characterized by EPR, ENDOR and TRIPLE resonance spectroscopy. The data indicate a rapid conformational interconversion of the cyclohexene moiety (ring A in the anthracyclines). The low‐temperature structures could be assigned to half‐chair conformers
描述了与蒽环类相关的五种取代蒽醌的合成。这些化合物的单电子还原产生相应的半醌,其特征在于 EPR、ENDOR 和三重共振光谱。数据表明环己烯部分(蒽环类中的环 A)的快速构象相互转换。低温结构可以分配给半椅式构象异构体,其分裂常数和扭转角通过简单的计算得到。与已发表的结果相反,在 4 位引入取代基,扰乱了蒽醌的对称性,导致自旋密度分布发生显着变化。介绍了已知蒽醌自由基的重新解释和分配。