Visible-light-mediated Minisci C-H alkylation of heteroarenes with unactivated alkyl halides using O2 as an oxidant
Herein, we report a protocol for direct visible-light-mediated Minisci C-H alkylation of heteroarenes with unactivated alkyl halides using molecular oxygen as an oxidant at room temperature. This mild protocol is compatible with a wide array of sensitive
Radical-based regioselective C-H functionalization of electron-deficient heteroarenes: Scope, tunability, and predictability
Radical addition processes can be ideally suited for the direct functionalization of heteroaromatic bases, yet these processes are only sparsely used due to the perception of poor or unreliable control of regiochemistry. A systematic investigation of fact
O'Hara, Fionn,Blackmond, Donna G.,Baran, Phil S.
supporting information
p. 12122 - 12134
(2013/09/02)
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