Evaluation of Reaction Conditions for Cu-Catalyzed Tertiary Alkylation of β-Allenyl Silane α
Copper-Catalyzed Cross-Nucleophile Coupling of β-Allenyl Silanes with Tertiary C-H Bonds: A Radical Approach to Branched 1,3-Dienes
Table 1
Once determining the β-allenyl silane 1a as the model substrate, we centered on evaluating the reaction parameters with low-cost copper salts. Through extensive screening of copper salts with different counterions and oxidant states (Table 1, entries 1−6), it was found that CuBr2 showed the best performance. Extra addition of phosphine (entry 7) or nitrogen (entry 8) ligands did not improve the conversion.
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