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Disulfoxide-palladium-catalyzed Oxidative Allylic C-H Amination

Posted on:2018-12-31Degree:MasterType:Thesis
Country:ChinaCandidate:L LiFull Text:PDF
GTID:2321330515970303Subject:Biochemical Engineering
Abstract/Summary:PDF Full Text Request
In recent years, the transition metal catalyzed coupling reactions for C-N bond formation, including alkenyl, aryl, allyl and alkyl of C-N bond reactions have been made some progress, and applications in in the total synthesis and Drug Synthesis.Challenging substrates and conditions in homogeneous catalysis usually pose a very stringent demands on the ligands used. In this paper, 12 novel disulfoxide ligands were designed and synthesized, and the best 1-adamantyl-substituted disulfoxide ligand was screened out. The catalyst permits the allylic oxidative C-N coupling reaction to proceed at lower catalyst loading (2 mmol%) while requiring smaller excess of reagents. Additionally, this ligand improves the availability and the yields of the C-N bond coupled substrate,a substrate that permits deprotection under both acidic and basic conditions, is used.
Keywords/Search Tags:C-N bond activation, Disulfoxide, Palladium catalyzed, C-N bond, Allylic C-H bond Amination
PDF Full Text Request
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