化学
选择氟
乙腈
亚甲基
酮
转化(遗传学)
有机化学
药物化学
催化作用
生物化学
基因
作者
Stojan Stavber,Igor Pravst,Marko Zupan
出处
期刊:Synthesis
[Georg Thieme Verlag KG]
日期:2005-01-01
卷期号:2005 (18): 3140-3146
被引量:10
标识
DOI:10.1055/s-2005-918424
摘要
Selective and efficient synthesis of α,α-difluoro ketones was achieved following a protocol which includes the transformation of α-methylene ketones to the corresponding n-butylimine derivatives and their further treatment with SelectfluorTM F-TEDA-BF4 in acetonitrile solution at 80 °C.
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