机译:通过闭环易位合成取代的吡啶和哒嗪
Department of Chemistry, University of Oxford, Chemistry Research Laboratory, Mansfield Road, Oxford, UK 0X1 3TA;
Department of Chemistry, University of Oxford, Chemistry Research Laboratory, Mansfield Road, Oxford, UK 0X1 3TA;
Department of Chemistry, University of Oxford, Chemistry Research Laboratory, Mansfield Road, Oxford, UK 0X1 3TA;
Department of Chemistry, University of Oxford, Chemistry Research Laboratory, Mansfield Road, Oxford, UK 0X1 3TA;
GlaxoSmithKline Research & Development Limited, Medicines Research Centre, Gunnels Wood Road, Stevenage, Hertfordshire,UKSGI 2NY;
Department of Chemistry, University of Oxford, Chemistry Research Laboratory, Mansfield Road, Oxford, UK 0X1 3TA;
机译:面向光学活性取代的环戊烷稠合碳环和氧环中型环的多样性取向合成研究:Grubbs-II催化的闭环烯烃复分解与闭环羰基烯烃复分解之间的竞争
机译:闭环复分解法合成2,4-取代的吡唑并[1,5-a]吡啶和吡唑并[1,5-a] a
机译:闭环复分解法合成2,4-取代的吡唑并[1,5-a]吡啶和吡唑并[1,5-a] a
机译:膦酸环和含NHC钌 - 茚基(双)吡啶配合物的闭环复分解中的合成与活性
机译:降冰片烯衍生物的高区域选择性开环/交叉易位和开环/闭环易位及其在角蛋白的全合成和酸敏感离子通道抑制剂的合成中的应用
机译:全合成抗肿瘤药抗生素(±)-链霉菌素:从头合成吡啶的第一代和第二代途径使用闭环复分解
机译:烯烃复合物配位球体中烯烃取代吡啶的闭合复分解的模板定向合成甲状腺炎。