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C. Wade Downey Sarah E. CovingtonDerek C. Obenschain Evan HallidayJames T. Rague Danielle N. Confair 《Tetrahedron letters》2014
para-Methoxybenzyl methyl ether acts as an alkylating agent for thiols in the presence of trimethylsilyl trifluoromethanesulfonate and trialkylamine base in good yields (58–96%). Aryl ketones are alkylated under similar conditions, probably through an enol silane intermediate, also in high yields (67–95%). The active alkylating species is likely a p-methoxybenzyl cation. 相似文献
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