
Wittig reaction - Wikipedia
Wittig reactions are most commonly used to convert aldehydes and ketones to alkenes. [1][2][3] Most often, the Wittig reaction is used to introduce a methylene group using …
Wittig反应 | 羰基制备烯烃_叶立德 - 搜狐
2021年4月10日 · Geissler研究了五价磷的化学性质,描述了甲基三苯磷 ( Ph3P=CH2 )与二苯甲酮的反应,定量 生成 1,1-二苯 乙烯 和三苯氧 膦 ( Ph 3 P= O)。 Wittig认识到这一发现的重要 …
有机人名反应——Wittig反应(维蒂希反应) - 知乎专栏
Wittig反应(维蒂希反应)是醛或酮与 磷叶立德 (Wittig试剂)发生亲核加成生成烯烃反应,该反应由德国化学家 Georg Wittig 在1954年发现,为此他获得了1979年的 诺贝尔化学奖。 Wittig …
The Wittig Reaction - Chemistry LibreTexts
2023年1月23日 · Organophosphorus ylides react with aldehydes or ketones to give substituted alkenes in a transformation called the Wittig reaction. This reaction is named for George Wittig …
Wittig Reaction - Examples and Mechanism - Master Organic …
2018年2月6日 · Below is a useful reaction called the Wittig reaction that achieves this transformation. It won its inventor, Georg Wittig, the 1979 Nobel Prize in Chemistry (along with …
Methylenetriphenylphosphorane - Wikipedia
Methylenetriphenylphosphorane is an organophosphorus compound with the formula Ph 3 PCH 2. It is the parent member of the phosphorus ylides, popularly known as Wittig reagents. It is a …
Triphenylphosphine - Wikipedia
Triphenylphosphine (IUPAC name: triphenylphosphane) is a common organophosphorus compound with the formula P (C 6 H 5) 3 and often abbreviated to P Ph 3 or Ph 3 P.
维蒂希反应(Wittig反应) - 百度文库
最简单的维蒂希试剂是亚甲基三苯基膦(Ph3P+−C−H2),是一个橙黄色固体,对空气和水都不稳定,可通过三苯基膦和溴甲烷生成的溴化三苯基甲基鏻 Ph3P+-CH3·Br−在干燥乙醚和氮气流 …
The Wittig Reaction - Chemistry LibreTexts
2025年2月24日 · A common Wittig reagent is methylenetriphenylphosphorane (Ph 3 P=CH 2) which is synthesized by reacting Triphenyl phosphine with methylbromide followed by …
常用试剂—-亚甲基三苯基膦烷 – 化学慧
【结构式】 Ph3P=CH2 【物理性质】 白色晶体,mp 96 oC。溶于醚、 THF、DME、苯、甲苯、DMSO。水或者质子溶剂会将该试剂彻底破坏。 【制备和商品】 该试剂无法作为商品购得, …