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Ethylene derivatives aldehydes 2 molecules

Zirconacyclopentene 1-5 could also be applied in synthetic reaction (Scheme 1.8). For example, in the presence of CuCl and iodine, oxidative demetallation of 1-5 gives cyclobutene derivatives [34]. Reaction of 1-5 with acid chloride gives tri-subslimted cyclopentadiene derivatives [35]. This research group also reported zirconocene-mediated cyclization of alkyne, ethylene, and two molecules of aldehyde toward synthesis of 2-alkenyl tetrahydrofuran [36]. [Pg.18]

The ethylene diamine-dextran derivative may be used for the coupling of carboxylate-contain-ing molecules by the carbodiimide reaction, for the coupling of amine-reactive probes, or to modify further using heterobifunctional crosslinkers. The hydrazide-dextran derivative may be used to crosslink aldehyde-containing molecules, such as oxidized carbohydrates or glycoproteins. [Pg.956]

Synthetic precursors for aliphatic materials mirror the pattern of their naturally derived counterparts in that the commonest units are even in carbon chain length. This is because they are usually derived from ethylene through oligomerisation. Thus, coupling of two ethylene molecules produces a four-carbon chain, three produces six, and so on. In order to obtain an odd number of carbon atoms in the chain, one of the simplest techniques is to add a single carbon to an even chain which can be achieved, for example, by hydroformylation. Hydroformylation also introduces an alcohol function and opens the way for oxidation to aldehydes and acids. Three carbon units are available from propylene as well as by reaction of ethylene with a one-carbon unit. [Pg.125]

Vinyl Alcohol, CH2 = CHOH, which is the hydroxyl derivative of ethylene, has never been isolated. Reactions which should produce a compound of this structure lead to the formation of aldehyde it is probable that vinyl alcohol is first produced, and that aldehyde is formed by a rearrangement of the atoms in the molecule —... [Pg.105]


See other pages where Ethylene derivatives aldehydes 2 molecules is mentioned: [Pg.501]    [Pg.746]    [Pg.376]    [Pg.401]    [Pg.324]    [Pg.251]    [Pg.230]    [Pg.365]    [Pg.591]    [Pg.49]    [Pg.118]    [Pg.103]    [Pg.241]    [Pg.154]    [Pg.388]    [Pg.187]    [Pg.384]    [Pg.411]   


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