4028-23-3Relevant articles and documents
Diastereoselective synthesis of trisubstituted olefins using a silicon-tether ring-closing metathesis strategy
Prunet, Jo?lle,Tiniakos, Alexander F.,Wittmann, Stéphane
, p. 2297 - 2306 (2020/04/03)
The diastereoselective synthesis of trisubstituted olefins with concomitant C-C bond formation is still a difficult challenge, and olefin metathesis reactions for the formation of such alkenes are usually not high yielding or/and diastereoselective. Herein we report an efficient and diastereoselective synthesis of trisubstituted olefins flanked by an allylic alcohol, by a silicon-tether ring-closing metathesis strategy. Both E- and Z-trisubstituted alkenes were synthesised, depending on the method employed to cleave the silicon tether. Furthermore, this methodology features a novel Peterson olefination for the synthesis of allyldimethylsilanes. These versatile intermediates were also converted into the corresponding allylchlorodimethylsilanes, which are not easily accessible in high yields by other methods.
METHOD OF PREPARING ALLYLCHLOROSILANE DERIVATIVE
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Page/Page column 4, (2011/06/23)
Provided is a method of preparing allylchlorosilane, and more particularly, a method of preparing allylchlorosilane with high yield by Si—C coupling reaction of an allyl chloride derivativce with a hydrosilane derivative under specific reaction conditions without using a catalyst.
Method for obtaining halogenated monoorganoxysilanes useful in particular as synthesis intermediates
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Page/Page column 8, (2008/06/13)
The invention concerns the preparation of halogenated monoorganoxysilanes, of formula (I), said compounds being useful as synthesis intermediate in organic chemistry. Said method for preparing monoorganoxysilanes consists in: using as starting product halogenoalkylsilanes of the (CH3)2SiCl2 type and in substituting the silicon with a radical bearing a divalent unit bound to an electrophilic reactive group capable of reacting with at least an appropriate nucleophilic agent to form a functionalised monoorganoxysilane of formula (II) with, for example: R=C1-C4 alkyl; R, R=C1-C6 alkyl; B═C1-C10 alkylene; m=1 or 2; Hal=halogen; W=amino, mercapto, (organosilyl)-organopolythio radical.
