BSTFA公司
重氮甲烷
化学
吡啶
硅胶
试剂
硅烷化
高效液相色谱法
烷基
甲苯
反应性(心理学)
乙酰胺
色谱法
有机化学
核化学
高分子化学
药物化学
衍生化
催化作用
病理
替代医学
医学
标识
DOI:10.1080/01483918808082260
摘要
Abstract Several trimethylsilyl (TMS) donors including bis-N, O-trimethylsilylacetamide (BSA), bis-N, O-trimethylsilyltrifluoro-acetamide (BSTFA), hexamethyldisilane (HMDS), trimethylchlorosilane (TMCS) with and without pyridine, 2-trimethylsiloxypent-2-en-A-one (TMSOP), trimethylsilyldimethylamine (TMSDMA), and trimethylsilylimidazole (TMSIM) were reacted with 60 Å silica. TMSIM at 60°C with reaction times of one hour or less gave coverage of silica gel equivalent to that provided by refluxing TMCS and pyridine in toluene for 67 hrs. Reactivity of the TMS donors studied may be ranked in the following order: TMSIM > TMSDMA > BSTFA > BSA > TMCS > TMSOP > HMDS. TMSIM appears to be the reagent of choice for end-capping of alkyl bonded HPLC phases.
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