Useful Synthesis of Fragment A–C–D of a Thiostrepton-type Macrocyclic Antibiotic, Thiocilline I
                                
                                    
                                        作者:Shuusuke Suzuki、Yasuchika Yonezawa、Chung-gi Shin                                    
                                    
                                        DOI:10.1246/cl.2004.814
                                    
                                    
                                        日期:2004.7
                                    
                                    Useful synthesis of the main Fragment A–C–D segment constructing a thiostrepton-type macrocyclic antibiotic, thiocilline I, was first achieved by coupling of the 2,3,6-polythiazolesubstituted pyridine skeleton (Fragment A–C) with Fragment D.
                                    通过将2,3,6-多
噻唑基取代
吡啶骨架(片段A-C)与片段D偶联,首次实现了构建
硫霉素类大环抗生素
硫环素I的主要片段A-C-D的有用合成。