catalyst is developed. The reaction is applicable to various nitrogen‐containing heterocycles. The exceptionally high functional group compatibility of this method was confirmed by the oxidation of an unprotected dihydroindolactam V to indolactam V. Furthermore, by taking advantage of the oxygen‐mediated structural change of the Grubbs catalyst, we integrated ring‐closing metathesis and subsequent aerobic
开发了由Grubbs催化剂催化的含氮杂环的好氧脱氢。该反应适用于各种含氮杂环。未保护的二氢
吲哚内酰胺V氧化为
吲哚内酰胺V证实了该方法具有极高的官能团相容性。此外,利用氧介导的Grubbs催化剂的结构变化,我们整合了闭环复分解和随后的需氧脱氢以分子氧为
化学触发物开发新型辅助串联催化。所述辅助串联催化的效用通过的简明合成证明Ñ含稠合杂
芳烃包括天然抗生素,
绿脓菌素。