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机译:从炔丙醇轻松地一锅合成三种不同的取代噻唑
Department of Chemistry, College of Chemistry and Chemical Engineering,and State Key Laboratory for Physical Chemistry of Solid Surfaces,Xiamen University, Xiamen 361005, Fujian, P. R. China;
rnDepartment of Chemistry, College of Chemistry and Chemical Engineering,and State Key Laboratory for Physical Chemistry of Solid Surfaces,Xiamen University, Xiamen 361005, Fujian, P. R. China;
rnDepartment of Chemistry, College of Chemistry and Chemical Engineering,and State Key Laboratory for Physical Chemistry of Solid Surfaces,Xiamen University, Xiamen 361005, Fujian, P. R. China;
rnDepartment of Chemistry, College of Chemistry and Chemical Engineering,and State Key Laboratory for Physical Chemistry of Solid Surfaces,Xiamen University, Xiamen 361005, Fujian, P. R. China;
rnDepartment of Chemistry, College of Chemistry and Chemical Engineering,and State Key Laboratory for Physical Chemistry of Solid Surfaces,Xiamen University, Xiamen 361005, Fujian, P. R. China;
机译:布朗斯台德酸与硫代酰胺催化炔丙醇的环化反应。轻松合成二取代和三取代的噻唑
机译:布朗斯台德酸催化取代炔丙醇合成1,5-烯炔和双环[3.1.0]己烯的一锅合成
机译:通过炔丙基酰肼从炔丙基醇轻松地一锅合成3,5-二取代的1 h-吡唑
机译:钌和金催化串联反应:从丙基醇和酰胺的合成取代的恶唑
机译:第一部分:仲醇的一锅法合成和仲炔丙醇的一锅法不对称合成。第二部分仲炔丙醇的氧化还原异构化为烯酮。第三部分(+)-discodermolide C9-C14片段的合成研究。第四部分聚丙烯酸酯天然产物的抗,抗立体三环构建基的不对称合成
机译:二氧化硅负载的钨硅酸作为可重复使用的催化剂由环境良性一锅法合成的新型取代的Hantzsch噻唑衍生物的合成及生物学评估
机译:从炔丙醇轻松地一锅合成三种不同的取代噻唑