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Enantioselective Synthesis of Complex Carbocycles by C-H Insertion of Aryl/Aryl Carbenes
Jose M Ruiz1, Dylan R Turner1, Mingchun Gao1
1Department of Chemistry, University of California, Davis, California 95616, United States.
Abstract:
A range of benzene and indole-fused carbocyclic molecules were accessed by the enantioselective C-H insertion of rhodium aryl/aryl carbenes. 1,4, 1,5, and 1,6 C-H insertion reactions are chemoselective for insertion into carbon centers appended with an electron-donating heteroatom. Examples include a range of ethers, a free hydroxyl group, and a range of nitrogen substituents, including basic amines. DFT calculations support a step-wise mechanism of this process and provide insight into the origin of both stereoselectivity and the preference for C-H versus O-H insertion.
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