Cationic Cobalt(III) Catalyzed Indole Synthesis: The Regioselective Intermolecular Cyclization of N-Nitrosoanilines and Alkynes

被引:179
作者
Liang, Yujie [1 ]
Jiao, Ning [1 ,2 ]
机构
[1] Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Xue Yuan Rd 38, Beijing 100191, Peoples R China
[2] Chinese Acad Sci, State Key Lab Organomet Chem, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
C-H activation; cobalt; indoles; reaction mechanisms; regioselectivity; C-H ACTIVATION; METALATION-DEPROTONATION MECHANISM; NITROGEN-CONTAINING HETEROCYCLES; OXIDATIVE ANNULATION; DIRECTED C(SP(2))-H; EFFICIENT SYNTHESIS; TERMINAL ALKYNES; DIAZO-COMPOUNDS; BOND-CLEAVAGE; AMIDATION;
D O I
10.1002/anie.201511002
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The unique regioselectivity and reactivity of cobalt(III) in the direct cyclization of N-nitrosoanilines with alkynes for the expedient synthesis of N-substituted indoles is demonstrated. In the presence of a cobalt(III) catalyst, high regioselectivity was observed when using unsymmetrical meta-substituted N-nitrosoanilines. Moreover, internal alkynes bearing electron-deficient groups, which are almost unreactive in the [Cp*Rh-III]-catalyzed system, display good reactivity in this transformation.
引用
收藏
页码:4035 / 4039
页数:5
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