1974
DOI: 10.1021/jo00938a037
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Facile one-step synthesis of 5-silaspiro[4.4]nona-2,7-diene

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Cited by 34 publications
(3 citation statements)
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“…Identification of 3-hexene was made by comparing its IR, NMR, and mass spectra with those of the authentic material after fractional distillation (45-68 °C) of the product. Identification of 2-butene was made using a fraction (bp [25][26][27][28][29][30][31][32][33][34][35][36][37][38][39][40] °C) which also contained the starting 2-pentene.…”
Section: Methodsmentioning
confidence: 99%
“…Identification of 3-hexene was made by comparing its IR, NMR, and mass spectra with those of the authentic material after fractional distillation (45-68 °C) of the product. Identification of 2-butene was made using a fraction (bp [25][26][27][28][29][30][31][32][33][34][35][36][37][38][39][40] °C) which also contained the starting 2-pentene.…”
Section: Methodsmentioning
confidence: 99%
“…Introduction to synthetic practice in 1972 of highly active Mg* (Rieke magnesium) [188] allowed direct metalation of buta-1,3-diene without preliminary chemical activation of magnesium. Buta-1,3-diene reacts with Mg* at room temperature to give the butadiene-magnesium reagent (MgC 4 H 6 ) n 132, which vigorously react with SiCl 4 yielding 5-silaspiro-4,4 0 -nona-1,7-dien 143 [189].…”
Section: Thfmentioning
confidence: 99%
“…The synthesis of authentic materials, of course, made possible the identification of the l-sila-3-cyclopentene [203] and the silaspirononadiene [204] shown above. The finding that this silacyclopentene can be formed in high yield can be seen that methylsilane is 1.12 to 1.35 times as reactive as silane in producing the products expected from silylene insertion into a silicon-hydrogen bond.…”
Section: The Relationship Between Hot Atom Experiments and Thermal Rementioning
confidence: 99%