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4- Ethyl-l-hexene

Account for the fact that addition of CBrC in the presence of peroxides takes place faster to 2-ethyl-l-hexene than to 1-octene. [Pg.222]

Similar unsatisfactory results, usually with even lower inductions are obtained with other terminal aliphatic alkenes such as 1-pentene, 2-methy]-l -butene, 3-methyl-l -butene, 2,3-dimethyl-l-butene, 3,3-dimethyl-l-butene, 2,3,3-trimethyl-l-butene, 2-ethyl-l-hexene, I-hex-ene and 1-octene (Table 1). [Pg.321]

A 2-ethyl-l-hexene B 3-methyl-l-heptene C 5-methyl-2-heptene D 2-octene... [Pg.549]

Ethylene glycol, polyester use, 479-481, 489 Ethylene glycol disorbate, polyester reactions, 507 Ethylene oxide, MA polycondensation, 482, 483 Ethylene sulfite, MA polycondensation, 483 Ethylenimine, MA polycondensation, 516 2-Ethylhexanoate peroxide, 293 2-Ethylhexenal, A-phenylmaleiamic Diels-Alder adduct, 110 2-Ethyl-l-hexene... [Pg.835]

Carbon dioxide, 2-ethyl-l-hexene, 2-ethyI-l-hexanol 103... [Pg.488]

As shown in Scheme 1.30, the chiral titanocene catalyst 34 hydrogenates unfimctionalized, disubstituted styrenes under 136 atm of hydrogen at 65°C to give the saturation products with 83 to >99% ee [156]. A high enantioselectivity is now realized only with aiyl-substituted olefins. The enantioselectivity of 41% ee attained 2-ethyl-l-hexene and 34 as catalyst is the highest for hydrogenation of non-arwnatic olefins. [Pg.32]


See other pages where 4- Ethyl-l-hexene is mentioned: [Pg.59]    [Pg.311]    [Pg.314]    [Pg.321]    [Pg.118]    [Pg.84]    [Pg.161]    [Pg.1682]    [Pg.635]    [Pg.533]    [Pg.198]    [Pg.34]    [Pg.392]    [Pg.1367]    [Pg.390]    [Pg.396]    [Pg.18]    [Pg.163]    [Pg.24]    [Pg.118]    [Pg.1264]    [Pg.18]    [Pg.301]    [Pg.342]    [Pg.119]    [Pg.89]    [Pg.90]    [Pg.91]   
See also in sourсe #XX -- [ Pg.313 ]




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2-Ethyl-2-hexen

2-Ethyl-2-hexenal

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