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Platinum(II)-Catalyzed Asymmetric Ring-Opening Addition of Arylboronic Acids to Oxabenzonorbornadienes

机译:铂(II)催化芳基硼酸到氧杂苯并降冰片二烯的不对称开环加成反应

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摘要

A new platinum(II)-catalyzed asymmetric ring-opening addition of arylboronic acids to oxabenzonorbornadienes was developed, which afforded the corresponding cis-2-aryl-1,2-dihydronaphthalen-1-ol products in high yields (up to 97%) with moderate to good enantioselectivities (up to 89% ee) under very mild conditions. The effects of various ligands, catalyst loading, bases, solvents, and temperatures on the yield and enantioselectivity of the reaction were also investigated. The cis configuration of product 2m was confirmed by X-ray diffraction analysis. A potential mechanism for the present catalytic reaction is proposed.
机译:开发了一种新的铂(II)催化的芳基硼酸不对称开环加成芳基苯并降冰片二烯,从而以高收率提供了相应的顺式-2-芳基-1,2-二氢萘-1-醇产物(高达97%)在非常温和的条件下具有中等至良好的对映选择性(高达89%ee)。还研究了各种配体,催化剂负载量,碱,溶剂和温度对反应产率和对映选择性的影响。通过X射线衍射分析确认产物2m的顺式构型。提出了本催化反应的潜在机理。

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