1,2,9,16,17,24-hexathia[2.1.2.1]-4,6,8,11,13,15,19,21,23,26,28,30-dodecamethyl-metacyclophane
作者:F. Bottino、S. Foti、S. Pappalardo
DOI:10.1016/0040-4020(77)80115-4
日期:1977.1
The synthesis of 1,2,9,16,17,24 - hexathia[2.1.2.1] - 4,6,8,11,13,15,19,21,23,26,28,30 - dodecamethyl - metacyclophane by direct sulphuration of mesitylene, the first report of a single-step synthesis of an aromatic macrocycle with alternating sulphide and disulphide linkages, is reported. Structure determination of this compound was achieved by mass spectrometry, and by reductive degradation to 3
1,2,9,16,17,24-hexathia [2.1.2.1]-4,6,8,11,13,15,19,21,23,26,28,30-十二甲基-偏环环烷的合成报道了对亚甲基三甲苯直接硫化,这是一步式合成具有交替的硫化物和二硫键的芳香族大环化合物的报道。该化合物的结构测定是通过质谱法,以及通过还原降解为3,3'-二硫代-二巯基亚砜和将后者再氧化为原始大环化合物来实现的。据报道有关大环形成的可能途径的一些证据。