Reactions of tetramesityldisilene with acid chlorides and ketenes
Reactions of tetramesityldisilene with acid chlorides and ketenes
复制标题
四均三硅烯与酰基氯和乙烯酮的反应
DOI:
10.1021/om00030a029
复制
发表时间:
1993
期刊:
影响因子:
2.8
通讯作者:
R. West
中科院分区:
文献类型:
--
作者:
A. Fanta;J. Belzner;D. Powell;R. West
Tetramesityldisilene (1) reacts with dimethylketeneand diphenylketene by [2+ 2] cycloaddition to the carbonyl group to give 3-methylidene-1, 2-disilaoxetanes, 4b and 4c. Acetyl and dimethylacetyl chlorides react with 1 with elimination of HC1 to give similar products, 4a and 4b, along with 1, 1, 2, 2-tetramesityl-l-chlorodisilane (3). Nonenolizable acid chlorides react variously with 1: Heptafluorobutyryl chloride gives the [2+ 2] cycloaddition product, 11; trimethylacetyl chloride undergoes a slow reaction to give 3 and iso-butene; 3, 4, 5-trimethox-ybenzoyl chloride produces 25% of a [2+ 4] cycloaddition product, 14. The X-ray crystal structure of 4b was determined: triclinic, PI, Z= 2, with cell dimensions a= 10.442 (2) k, b= 11.123 (2) A, c= 16.124 (3) k, a= 78.06 (3), ß= 87.93 (3), and y= 72.94 (3).