A cobalt-catalyzed ring-opening/hydroxylation cascade of highly strained cyclopropanols has been developed for the first time. The reaction was conducted under open-air atmosphere to afford a broad series of structura...A cobalt-catalyzed ring-opening/hydroxylation cascade of highly strained cyclopropanols has been developed for the first time. The reaction was conducted under open-air atmosphere to afford a broad series of structurally diverse β-hydroxy ketones in moderate to good yields with high regioselectivity.The protocol features mild reaction conditions, simple operation, high-functional-group tolerance, facile scalability, and heterocycle compatibility.展开更多
We have developed a metal-free radical cascade reaction of N-substituted 2-aryl indoles with readily available sulfonyl hydrazides for the rapid construction of arylsulfonyl-substituted indolo[2,1-a]isoquinolin-6(5H)-...We have developed a metal-free radical cascade reaction of N-substituted 2-aryl indoles with readily available sulfonyl hydrazides for the rapid construction of arylsulfonyl-substituted indolo[2,1-a]isoquinolin-6(5H)-one derivatives.With the TBAI–TBHP catalytic system,a broad series of structurally diverse indolo[2,1-a]isoquinolin-6(5H)-one derivatives were obtained in moderate to excellent yields.The reaction features mild reaction conditions,operationally easiness,scaled-up feasibility,and high functional-group-tolerance.展开更多
基金State Key Basic Research Program of the People's Republic of China(No.2018YFC0310900)National Natural Science Foundation of China(Nos.21871018,21732001)+9 种基金Shenzhen Science and Technology Innovation Committee(Nos.KQTD20190929174023858,JCYJ20180504165454447)Industry and Information Technology Bureau of Shenzhen Municipality(No.201806151622209330)Guangdong Science and Technology Program(No.2017B030314002)Shenzhen-Hong Kong Institute of Brain Science-Shenzhen Fundamental Research Institutions(No.2019SHIBS0004)the National Ten Thousand Talent Program(the Leading Talent Tier)for the financial supportthe Science and Technology Project of Henan Province(No.202102310328)the PhD Start-up Program of Anyang Institute of Technology(No.BSJ 2021042)Guangzhou Basic and Applied Basic Research Project in China(Nos.202102020134,202102020690)Youth Innovation Talents Project of Guangdong Universities(natural science)in China(No.2019KQNCX098)the Henan Postdoctoral Foundation and the Postdoctoral Innovation Base of Anyang Institute of Technology for financial support。
文摘A cobalt-catalyzed ring-opening/hydroxylation cascade of highly strained cyclopropanols has been developed for the first time. The reaction was conducted under open-air atmosphere to afford a broad series of structurally diverse β-hydroxy ketones in moderate to good yields with high regioselectivity.The protocol features mild reaction conditions, simple operation, high-functional-group tolerance, facile scalability, and heterocycle compatibility.
基金the State Key Basic Research Program of the People’s Republic of China (No. 2018YFC0310900)National Natural Science Foundation of China (Nos. 21871018, 21801005, 21732001)+7 种基金Shenzhen Science and Technology Innovation Committee (Nos. KQTD20190929174023858, JCYJ20180504165454447)Industry and Information Technology Bureau of Shenzhen Municipality (No. 201806151622209330)Guangdong Science and Technology Program (No. 2017B030314002)Shenzhen-Hong Kong Institute of Brain Science-Shenzhen Fundamental Research Institutions (No. 2019SHIBS0004)the National Ten Thousand Talent Program (the Leading Talent Tier) for the financial supportthe Science and Technology Project of Henan Province (No. 202102310328)the Henan Postdoctoral Foundationthe Postdoctoral Innovation Base of Anyang Institute of Technology for financial support
文摘We have developed a metal-free radical cascade reaction of N-substituted 2-aryl indoles with readily available sulfonyl hydrazides for the rapid construction of arylsulfonyl-substituted indolo[2,1-a]isoquinolin-6(5H)-one derivatives.With the TBAI–TBHP catalytic system,a broad series of structurally diverse indolo[2,1-a]isoquinolin-6(5H)-one derivatives were obtained in moderate to excellent yields.The reaction features mild reaction conditions,operationally easiness,scaled-up feasibility,and high functional-group-tolerance.
