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Manganese-Catalyzed ortho-C-H Amidation of Weakly Coordinating Aromatic Ketones
Organic Letters ( IF 4.9 ) Pub Date : 2018-07-16 00:00:00 , DOI: 10.1021/acs.orglett.8b01770
Xianqiang Kong 1 , Bo Xu 1
Affiliation  

An efficient manganese-catalyzed ortho-C-H amidation of weakly coordinating aromatic ketones using the readily available sulfonyl azide as the amination reagent is developed. The key step is the ketone directed aromatic metalation using the in situ generated reactive Mn intermediate, MnMe(CO)5. This method offers excellent chemical yields, high regioselectivities, and good functional group tolerance.

中文翻译:

弱配位芳香族酮的锰催化邻位-CH酰胺化

开发了使用易得的磺酰叠氮化物作为胺化试剂的弱配位芳族酮的有效锰催化邻位-CH酰胺化反应。关键步骤是使用原位生成的反应性Mn中间体MnMe(CO)5进行的酮基定向芳族金属化。该方法具有出色的化学收率,高区域选择性和良好的官能团耐受性。
更新日期:2018-07-16
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