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Download fileDesign, Synthesis, and Validation of an Effective, Reusable Silicon-Based Transfer Agent for Room-Temperature Pd-Catalyzed Cross-Coupling Reactions of Aryl and Heteroaryl Chlorides with Readily Available Aryl Lithium Reagents
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posted on 2016-02-02, 00:00 authored by Dionicio Martinez-Solorio, Bruno Melillo, Luis Sanchez, Yong Liang, Erwin Lam, K. N. Houk, Amos B. SmithA reusable silicon-based transfer
agent (1) has been
designed, synthesized, and validated for effective room-temperature
palladium-catalyzed cross-coupling reactions (CCRs) of aryl and heteroaryl
chlorides with readily accessible aryl lithium reagents. The crystalline,
bench-stable siloxane transfer agent (1) is easily prepared
via a one-step protocol. Importantly, this “green” CCR
protocol circumvents prefunctionalization, isolation of organometallic
cross-coupling partners, and/or stoichiometric waste aside from LiCl.
DFT calculations support a σ-bond metathesis mechanism during
transmetalation and lead to insights on the importance of the CF3 groups.
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TransferinsightmetathesiCCRaryl lithium reagentsCF 3 groupstransfermechanismorganometallicHeteroaryl ChloridesImportantlySynthesiReusableEffectivetransmetalationimportancesiloxaneLiClheteroaryl chloridesstoichiometricValidationprefunctionalizationisolationAgentDFT calculations supportAvailable Aryl Lithium ReagentsAbond