2002
DOI: 10.1002/1615-4169(200212)344:10<1142::aid-adsc1142>3.0.co;2-p
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Platinum-Catalysed Hydrosilylation of Unsaturated Fatty Acid Esters

Abstract: Different Pt(IV), Pt(II) and Pt(0) catalysts were screened for the hydrosilylation of fatty acid esters containing terminal as well as internal double bonds. The reaction of terminally unsaturated fatty acid esters proceeded smoothly with short reaction times for nearly all examined catalysts, whereas Pt(IV) species and Pt(II) or Pt(0) species with labile ligands were sufficiently active in the reaction of internally unsaturated compounds. For methyl linoleate, a conjugation of the two internal double bonds be… Show more

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Cited by 71 publications
(25 citation statements)
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“…Hydrosilylation has already been applied to unsaturated fatty acids [36][37][38][39] and has been used to prepare main chain flexible polybenzoxazines [40][41][42]. In this work, two difunctional silanes having different SiAH reactivity were used: 1,1,3,3-tetramethyldisiloxane S1 and 1,4-phenylene-bis-dimethylsilane S2 (Scheme 2).…”
Section: Ax-bis-benzoxazine Synthesis(b1-3s1 B1-3s2)mentioning
confidence: 99%
“…Hydrosilylation has already been applied to unsaturated fatty acids [36][37][38][39] and has been used to prepare main chain flexible polybenzoxazines [40][41][42]. In this work, two difunctional silanes having different SiAH reactivity were used: 1,1,3,3-tetramethyldisiloxane S1 and 1,4-phenylene-bis-dimethylsilane S2 (Scheme 2).…”
Section: Ax-bis-benzoxazine Synthesis(b1-3s1 B1-3s2)mentioning
confidence: 99%
“…Herein, we report a multi-step divergent synthesis of second generation siloxane ester dendrimers by using hydrosilation [38][39][40] and esterification reactions [41][42][43]. In the present work we have carried out the hydrosilation reaction of the Si-H functional G I A and G I B dendrimers with maleic anhydride to obtained anhydride functional dendrimers G I A p and G I B p (Scheme 1).…”
Section: Accepted Manuscriptmentioning
confidence: 99%
“…8. Isomeric silane adducts are formed as hydrosilylation products [26,27]. The conversions of linoleic acid methyl ester and the yields of the isomeric silyl adducts depend on the applied catalysts (Table 3).…”
Section: Hydrosilylationsmentioning
confidence: 99%