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Ethylidene, bridging

Drinkine, J., Lopes, P, Kennedy, J., Teissedre, P., Saucier, C. (2007a). Analysis of ethylidene-bridged flavan-3-ols in wine. J. Agric. Food Chem., 55, 1109-1116. [Pg.499]

One example of C-vinylation of an aromatic compound is the reaction of /7-tert-butyl-phenol and acetylene [47] to give ethylidene-bridged oligomers (eq. (21)), which are formed by dual attack of the aromatic compound on acetylene. The catalyst employed is zinc naphthenate. These products are used, inter alia, as vulcanizing auxiliaries in the tire industry. [Pg.282]

Waterhouse AL (2002) Wine phenolics. Ann N Y Acad Sci 957 21-36 Drinkine J, Lopes P, Kermedy JA, Teissedre P-L, Saucier C (2007) Analysis of ethylidene-bridged flavan-3-ols in wine. J Agric Food Chem 55 1109—1116... [Pg.2273]

Badia et al. designed and synthesized more than 30 huprines, which are the tacrine-HA hybrids of the 4-aminoquinoline moiety of tacrine combined with the bridged carbobicychc moiety, without the ethylidene substituents, of HA. Pharmacological studies of these compounds demonstrated that they are a novel class of potent and selective AChEIs. 3-Chloro-substituted huprines 49a and 49b are the... [Pg.165]

See other pages where Ethylidene, bridging is mentioned: [Pg.24]    [Pg.249]    [Pg.234]    [Pg.71]    [Pg.239]    [Pg.95]    [Pg.407]    [Pg.1915]    [Pg.1920]    [Pg.1921]    [Pg.2269]    [Pg.393]    [Pg.103]    [Pg.65]    [Pg.24]    [Pg.249]    [Pg.234]    [Pg.71]    [Pg.239]    [Pg.95]    [Pg.407]    [Pg.1915]    [Pg.1920]    [Pg.1921]    [Pg.2269]    [Pg.393]    [Pg.103]    [Pg.65]    [Pg.149]    [Pg.78]    [Pg.426]    [Pg.231]    [Pg.185]    [Pg.162]    [Pg.188]    [Pg.219]    [Pg.216]    [Pg.158]    [Pg.249]    [Pg.145]    [Pg.161]    [Pg.220]    [Pg.290]    [Pg.137]    [Pg.138]    [Pg.248]    [Pg.176]    [Pg.349]    [Pg.187]    [Pg.793]    [Pg.249]    [Pg.55]    [Pg.391]    [Pg.311]    [Pg.243]   
See also in sourсe #XX -- [ Pg.158 ]



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1 - ethylidene

Ethylidenation

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