甲基化
烷基化
吡唑
试剂
选择性
位阻效应
化学
组合化学
有机化学
生物化学
基因
催化作用
作者
Emma Yang,Derek M. Dalton
标识
DOI:10.1021/acs.joc.3c02841
摘要
The development of a highly selective N-methylation of pyrazole heterocycles using commercially available, bench-stable α-halomethylsilanes as masked methylating reagents is described. Sterically bulky α-halomethylsilanes significantly improve the selectivity of N-alkylation over traditional methylating reagents and readily undergo protodesilylation in the presence of a fluoride source and water to give N-methyl pyrazoles. Selectivities of 92:8 to >99:1 N1/N2 regioisomeric ratios were achieved with a range of pyrazole substrates in good yields.
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