2007
DOI: 10.1002/chin.200725171
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Unsaturated Five‐Membered Selenium—Silicon Containing Heterocycles Based on the Reactions of Selenium Di‐ and Tetrahalides with Diorganyl Diethynyl Silanes.

Abstract: The reactions of diethynyl silanes (I) and (VIII) with selenium di-or tetrahalides (chlorides and bromides), generated in situ, at room temperature proceed in a regio-and stereoselective manner to give two new classes of di-and tetrahalogenated 1,3-selenasilol derivatives. -(AMOSOVA*, S. V.; MARTYNOV, A. V.; MAHAEVA, N. A.; BELOZEROVA, O. V.; PENZIK, M. V.; ALBANOV, A. I.; YAROSH, O. G.; VORONKOV, M. G.; J. Organomet. Chem. 692 (2007) 5, 946-952; A. E. Favorsky Inst. Chem., Sib. Branch, Russ. Acad. Sci., Irkut… Show more

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Cited by 3 publications
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“…An early report revealed the formation of selenasilafulvenes from the reactions of SeX2 (X = Cl, Br) with diorganyl diethynylsilanes [32] and this methodology has been extended to germanium-containing systems [22]. These reactions proceed with chemo-, regio-and stereoselectivity in chloroform at room temperature [22,33]. The transannular addition of SeX2 to cis,cis-1,5-cyclooctadiene takes place chemo-and regio-selectively to give 2,6-dihalo-9-selenobicyclo[3.3.1]nonanes in high yields [23].…”
Section: Selenium Dihalidesmentioning
confidence: 99%
“…An early report revealed the formation of selenasilafulvenes from the reactions of SeX2 (X = Cl, Br) with diorganyl diethynylsilanes [32] and this methodology has been extended to germanium-containing systems [22]. These reactions proceed with chemo-, regio-and stereoselectivity in chloroform at room temperature [22,33]. The transannular addition of SeX2 to cis,cis-1,5-cyclooctadiene takes place chemo-and regio-selectively to give 2,6-dihalo-9-selenobicyclo[3.3.1]nonanes in high yields [23].…”
Section: Selenium Dihalidesmentioning
confidence: 99%
“…An early report revealed the formation of selenasilafulvenes from the reactions of SeX2 (X = Cl, Br) with diorganyl diethynylsilanes [32] and this methodology has been extended to germanium-containing systems [22]. These reactions proceed with chemo-, regio-and stereoselectivity in chloroform at room temperature [22,33]. The transannular addition of SeX2 to cis,cis-1,5-cyclooctadiene takes place chemo-and regio-selectively to give 2,6-dihalo-9-selenobicyclo[3.3.1]nonanes in high yields [23].…”
Section: Selenium Dihalidesmentioning
confidence: 99%
“…We performed the reactions of SeCl 2 and SeBr 2 with dimethyldiethynylsilane which led to the formation of 3,6-dihalo-4,4-dimethyl-1,4-selenasilafulvenes [2,3]. This reaction extended further to dialkyldiethynylsilanes and -germanes showed the way to new classes of heterocycles containing in the ring atoms of selenium and the elements of 16 group [4][5][6][7][8].…”
Section: Sementioning
confidence: 99%