Sila-Pharmaka,35 岁。[1] Sila-Substitution des Akarizids Fenbutatinoxid und einiger seiner Derivate: Synthese und Eigenschaften von Hexakis[(二甲基苯基甲硅烷基)甲基]二锡烷和三[(二甲基苯基甲硅烷基)甲基](1,2,4-三唑基-l-基)锡兰/西拉-Pharmaca,第 35 次通讯 [1] Sila-取代杀螨剂芬布丁氧及其部分衍生物:六[(二甲基苯基甲硅烷基)甲基]二锡氧烷和三[(二甲基苯基甲硅烷基)甲基]1,2,4-三唑-l的合成和性质-基)锡烷
Sila-Pharmaka,35 岁。[1] Sila-Substitution des Akarizids Fenbutatinoxid und einiger seiner Derivate: Synthese und Eigenschaften von Hexakis[(二甲基苯基甲硅烷基)甲基]二锡烷和三[(二甲基苯基甲硅烷基)甲基](1,2,4-三唑基-l-基)锡兰/西拉-Pharmaca,第 35 次通讯 [1] Sila-取代杀螨剂芬布丁氧及其部分衍生物:六[(二甲基苯基甲硅烷基)甲基]二锡氧烷和三[(二甲基苯基甲硅烷基)甲基]1,2,4-三唑-l的合成和性质-基)锡烷
Synthesis and Free Radical Addition Reactions of Tris[(phenyldimethylsilyl)methyl]tin Hydride
作者:Verónica I. Dodero、Terence N. Mitchell、Julio C. Podestá
DOI:10.1021/om020936b
日期:2003.2.1
synthesis of the new bulky tris[(phenyldimethylsilyl)methyl]tinhydride (9), tetrakis[(phenyldimethylsilyl)methyl]tin (5), and hexakis[(phenyldimethylsilyl)methyl]ditin (10) as well as some physical properties are described. The addition of hydride 9 to seven mono- and disubstituted alkynes under radical conditions indicates that these reactions take place with complete stereoselectivity. Full 1H, 13C
新的大体积三[[(苯基二甲基甲硅烷基)甲基]锡氢化物(9),四[[苯基二甲基甲硅烷基)甲基]锡(5)和六[[苯基二甲基甲硅烷基)甲基]二锡(10)的合成以及一些物理性质是描述。在自由基条件下将氢化物9加至七个单取代和二取代的炔烃表明这些反应以完全的立体选择性进行。包括完整的1 H,13 C,119 Sn和29 Si NMR特性。
TACKE R.; LINK M.; JOPPIEN H.; ERNST L., Z. NATURFORSCH., 41,(1986) N 9, 1123-1128
作者:TACKE R.、 LINK M.、 JOPPIEN H.、 ERNST L.
DOI:——
日期:——
Sila-Pharmaka, 35. Mitt. [1] Sila-Substitution des Akarizids Fenbutatinoxid und einiger seiner Derivate: Synthese und Eigenschaften von Hexakis[(dimethylphenylsilyl)methyl]distannoxan und Tris[(dimethylphenylsilyl)methyl](1,2,4-triazoI-l-yl)stannan / Sila-Pharmaca, 35th Communication [1] Sila-Substitution of the Acaricide Fenbutatinoxide and Some of its Derivatives: Synthesis and Properties of Hexakis[(dimethylphenylsilyl)methyl]distannoxane and Tris[(dimethylphenylsilyl)methyl]1,2,4-triazol-l-yl)stannane
作者:Reinhold Tacke、Matthias Link、Hartmut Joppien、Ludger Ernst
DOI:10.1515/znb-1986-0911
日期:1986.9.1
Abstract Starting from SnCl4. hexasila-fenbutatinoxide (2b) [a silicon analogue of the acaricide fenbutatinoxide (2b)] and its derivatives lb and 3b were prepared (SnCl4 → 1b → 2b -> 3b). The distannoxanes 2a and 2b were found to react very easily with H2O to give the corresponding stannols 4a and 4b, respectively. In solution (C6D6 or CDCl3) the equilibria 2a/2b + H2O ⇄ 2 4a/4b were observed (1H NMR)