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Bridged addition

The initial step of the OH-pinenes reaction has been investigated using density functional theory and ab initio methods by Fan et al. [147] (for a- and j8-pinenes) and Ramirez-Ramirez et al. [148] (for y3-pinene). Both studies considered site-specific and stereo-specific (anti and syn position relative to the -C(CH3)2-bridge) addition of OH to the pinene C=C bond, forming four adducts for each pinene. [Pg.199]

The temperature of the product wAien placed in storage is another important factor having an effect on caldng tendency [97,98,99,100]. Higher temperatures increase the chemical reactivity, such as the reevaporation of water, w ich results in recrystallization and formation of solid crystalline bridges. Addition-... [Pg.489]

CompatibiliTxr bridge addition of chemical coupling promoter 229... [Pg.229]

COMPATIBILIZER BRIDGE ADDITION OF CHEMICAL COUPLING PROMOTER... [Pg.229]

R = organic group, R boron substituted organic group, Y = hydrocarbon bridge. Additional metal substituted triorganotin halides are listed in Subsections 2.7 1.1.3 and 2.7.1.2. [Pg.491]

See other pages where Bridged addition is mentioned: [Pg.57]    [Pg.52]    [Pg.244]    [Pg.357]    [Pg.44]    [Pg.365]    [Pg.278]    [Pg.349]    [Pg.47]    [Pg.87]    [Pg.251]    [Pg.564]    [Pg.320]    [Pg.176]    [Pg.341]    [Pg.115]    [Pg.285]    [Pg.136]    [Pg.231]    [Pg.1886]    [Pg.141]    [Pg.160]   
See also in sourсe #XX -- [ Pg.32 , Pg.110 ]



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