Design, 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
datasetposted on 2016-02-02, 00:00 authored by Dionicio Martinez-Solorio, Bruno Melillo, Luis Sanchez, Yong Liang, Erwin Lam, K. N. Houk, Amos B. Smith
A 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.
TransferinsightmetathesiCCRaryl lithium reagentsCF 3 groupstransfermechanismorganometallicHeteroaryl ChloridesImportantlySynthesiReusableEffectivetransmetalationimportancesiloxaneLiClheteroaryl chloridesstoichiometricValidationprefunctionalizationisolationAgentDFT calculations supportAvailable Aryl Lithium ReagentsAbond