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A-Olefins s. Ethylene derivs terminal

C-2,7-Octadien-l-ylation 26, 827 Olefins s. Ethylene derivs. a-Olefins s. Ethylene derivs., terminal Oligomerization... [Pg.274]

Olefins s. Ethylene derivatives a-Olefins s. Ethylene derivatives, terminal Oligonucleotides, removal of 0-prolective groups 21, 25 —, solid-phase synthesis 19, 33 suppl. 21 Orgaiiometallic compounds (s. a. under individual metals. Metal complex compounds)... [Pg.263]

Olefins s. Ethylene derivatives a-Olefins s. Ethylene derivatives, terminal Oleic acid as reagent 16, 867 Oligopeptides... [Pg.264]

The procedure for oxidation of the sulfide to the sulfone is based on that reported earlier by Bordwell and Pitt. The synthetic utility of phenyl vinyl sulfone and sulfoxide derives not only from their ability to serve as excellent Michael acceptors toward such reagents as enolate anions and organometallics, but also as moderately reactive dienophiles in Diels-Alder reactions. " The resulting adducts, in turn, can be chemically modified so that these electron-deficient olefins serve as useful synthons for acetylene,ethylene,terminal olefins,vinylsilanes, and ketene in [4 + 2] cycloadditions. Phenyl vinyl sulfone undergoes ready cycloaddition to Danishefsky s diene in the first step of a protocol for the regiospecific y-alkylation of 2-cyclohexenones. Furthermore, the ready lithiation of phenyl... [Pg.197]

The required terminal olefins used as substrates for the hydroformylation, such as 1-pentene or 1-octene, are available in large scales and can be derived either from Sasol s Fischer-Tropsch process or from the shell higher olefins process (SHOP), respectively [43, 44]. Alternatively, trimerization or tetramerization of ethylene affords 1-hexene [45] or 1-octene [46]. Dimerization of butadiene in methanol in the presence of a Pd catalyst (telomerization) is another industrially used access for the manufacture of 1-octene [46]. 1-Octene can also be produced on a large scale from 1-heptene via hydroformylation, subsequent hydrogenation, and dehydration (Scheme 6.2) [44]. This three-step homologation route is also valuable for the production of those higher olefins that bear an odd number of C atoms. (X-Olefins can also be derived from internal olefins by cross-metathesis reaction with ethylene [47]. [Pg.531]


See other pages where A-Olefins s. Ethylene derivs terminal is mentioned: [Pg.253]    [Pg.186]    [Pg.390]    [Pg.585]    [Pg.585]   


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A Olefins

A-Olefins s. Ethylene derivatives

A-Olefins s. Ethylene derivatives terminal

Ethylene olefination

Ethylene terminal

Ethylene-a-olefins

Ethylene/1-olefin

Olefins derivatives

Olefins s. Ethylene derivatives

Olefins s. Ethylene derivs

Terminal olefins

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