恶唑啉
对映选择合成
卡宾
钌
化学
吡啶
齿合度
催化作用
配体(生物化学)
组合化学
立体化学
药物化学
金属
有机化学
受体
生物化学
作者
Long Li,Feng Han,Xin Nie,Yubiao Hong,Sergei I. Ivlev,Eric Meggers
标识
DOI:10.1002/anie.202004243
摘要
Abstract A strategy for expanding the utility of chiral pyridine‐2,6‐bis(oxazoline) (pybox) ligands for asymmetric transition metal catalysis is introduced by adding a bidentate ligand to modulate the electronic properties and asymmetric induction. Specifically, a ruthenium(II) pybox fragment is combined with a cyclometalated N‐heterocyclic carbene (NHC) ligand to generate catalysts for enantioselective transition metal nitrenoid chemistry, including ring contraction to chiral 2H‐azirines (up to 97 % ee with 2000 TON) and enantioselective C(sp 3 )−H aminations (up to 97 % ee with 50 TON).
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