Silylative decarbonylation: a new route to arylsilanes
作者:Jonathan D. Rich
DOI:10.1021/ja00197a058
日期:1989.7
procedure is tolerant of a variety of aromatic substituents, for example, alkyl, halo, nitro, cyano, imide, acid anhydride, etc., and the synthesis of several new substituted aromatic chlorosilanes containing benzoyl chloride and phthalic anhydride moieties is described. Chloromethyldisilane starting reagents are available from the direct reaction of methyl chloride and silicon, making this methodology
RICH, JONATHAN D., J. AMER. CHEM. SOC., 111,(1989) N5, C. 5887-5893
作者:RICH, JONATHAN D.
DOI:——
日期:——
WANNAGAT, ULRICH;SCHRADER, ROLF, J. ORGANOMET. CHEM., 341,(1988) N 1-3, 95-108
作者:WANNAGAT, ULRICH、SCHRADER, ROLF
DOI:——
日期:——
Beiträge zur Chemie der Silicium-Stickstoffverbindungen
作者:Ulrich Wannagat、Rolf Schrader
DOI:10.1016/0022-328x(88)89066-1
日期:1988.3
2-(Chlorodimethylsilyl)benzoyl chloride, prepared in high yield from 2-(4-methoxyphenyldimethylsilyl)benzoic acid and thionyl chloride or phosphorus pentachloride, was investigated in its reaction with amines and alcohols. 1,1-Dimethyl-1-sila-isoindolin-3-one (from the reaction with ammonia) is a structural analogue of saccharin but, just as its lithium or sodium salt, it has no sweet taste at all