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A STUDY OF THE SILYLATION REACTION OF CYANOEPOXIDES WITH TRIMETHYLCHLOROSILANE IN THE PRESENCE OF MAGNESIUM | ||
| Journal of Sciences, Islamic Republic of Iran | ||
| مقاله 5، دوره 1، شماره 3، شهریور 1990 اصل مقاله (176.8 K) | ||
| چکیده | ||
| In the presence of magnesium and hexamethylphosphorictriamide, HMPT, trimethylchlorosilane, TMS-C1, reacts with cyanoepoxides to give related compounds. Ring cleavage at ? - position of cyanoepoxide, 1, followed by the addition of two trimethylsilyl groups leads to 2 then substitution of OSiMei by trimethylsilyl or H takes place to give ?, ? - bis (trimethylsilyl) nitrile or ? - trimethylsilylnitrile, respectively. Silylation reaction of cyanoepoxide 4 gives compounds 5 and 6, but silylation of 9 gives only ? - monosilylated derivative 10. Silylation of a, ?- diphenylcyanoepoxide, 11, leads to polysilylated products, by participation of both nitrile and epoxide functions | ||
| عنوان مقاله [English] | ||
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| چکیده [English] | ||
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آمار تعداد مشاهده مقاله: 955 تعداد دریافت فایل اصل مقاله: 950 |
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