1997
DOI: 10.1016/s1381-1169(96)00102-1
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The metathesis of 1-octene with the W(O-2,6-C6H3X2)2Cl4/R4Sn catalytic system

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Cited by 13 publications
(6 citation statements)
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“…This issue is essential because during the metathesis reaction a mixture of products can be formed due to alkene C-C double bond migration and isomerization which can occur both in substrates and products. These isomerisation products can also undergo a metathesis reaction, therefore in the reaction mixture three major groups of products can be identified (Scheme 1): primary metathesis products (PMP), isomerization products (IP) and secondary metathesis products (SMP), 33 which leads to a decrease in the yield of the desired products. Additionally, the side products resulting from unwanted isomerization, like monounsaturated hydrocarbons, α,ω-diesters, or monoesters with different chain lengths, 34 are frequently difficult to remove via standard purification techniques.…”
mentioning
confidence: 99%
“…This issue is essential because during the metathesis reaction a mixture of products can be formed due to alkene C-C double bond migration and isomerization which can occur both in substrates and products. These isomerisation products can also undergo a metathesis reaction, therefore in the reaction mixture three major groups of products can be identified (Scheme 1): primary metathesis products (PMP), isomerization products (IP) and secondary metathesis products (SMP), 33 which leads to a decrease in the yield of the desired products. Additionally, the side products resulting from unwanted isomerization, like monounsaturated hydrocarbons, α,ω-diesters, or monoesters with different chain lengths, 34 are frequently difficult to remove via standard purification techniques.…”
mentioning
confidence: 99%
“…The cocatalysts most frequently reported in the literature for [WCl 4 (OAr) 2 ] are aluminumalkyl and leadalkyl compounds. The literature contains few examples 11,19 of [WCl 4 (OAr) 2 ]-SnMe 4 , whose reactions were performed at 85 °C. Vosloo et al 19 reported that activity increased drastically from 50 to 65 °C in metathesis with the [WCl 4 (OAr) 2 ]-SnBu 4 system, although they found no activity at 50 o C for that system.…”
Section: Resultsmentioning
confidence: 99%
“…The literature contains few examples 11,19 of [WCl 4 (OAr) 2 ]-SnMe 4 , whose reactions were performed at 85 °C. Vosloo et al 19 reported that activity increased drastically from 50 to 65 °C in metathesis with the [WCl 4 (OAr) 2 ]-SnBu 4 system, although they found no activity at 50 o C for that system. Therefore, we repeated the reaction for [WCl 4 (O-C 6 H 3 Cl 2 ) 2 ] at 65 °C (Table 2).…”
Section: Resultsmentioning
confidence: 99%
“…Most significant of those are double‐bond isomerization and secondary metathesis of isomerized compounds. Therefore three major groups of products can be identified (Scheme ): primary metathesis products ( PMP ), isomerization products ( IP ) and secondary metathesis products ( SMP ) 7…”
Section: Introductionmentioning
confidence: 99%