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Ethyl acetate heterocyclic nitrogens

Addition compounds form with those organics that contain a donor atom, eg, ketonic oxygen, nitrogen, and sulfur. Thus, adducts form with amides, amines, and A/-heterocycles, as well as acid chlorides and ethers. Addition compounds also form with a number of inorganic compounds, eg, POCl (6,120). In many cases, the addition compounds are dimeric, eg, with ethyl acetate, in titanium tetrachloride-rich systems. By using ammonia, a series of amidodichlorides, Ti(NH2) Cl4, is formed (133). [Pg.131]

Hubert and co-workers have reported that alkyl diazoacetates react with A -diisopropylcarbodiimide in the presence of transition metal salts to give 2-isopropylimino-3-isopropyl-5-alkoxy-4-oxazolines.115 For example, treatment of ethyl diazoacetate with rhodium(II) acetate in the presence of A,A -diisopropylcarbodiimide (215) produced 2-iso-propylimino-3-isopropyl-5-ethoxy-4-oxazoline (217) in good yield. The formation of oxazoline 217 was interpreted in terms of an addition of ethoxycarbonylcarbene onto one of the nitrogen atoms of the carbodi-imide to give the transient ylide 216 which then cyclized to produce the observed heterocycle. [Pg.146]


See other pages where Ethyl acetate heterocyclic nitrogens is mentioned: [Pg.10]    [Pg.232]    [Pg.1008]    [Pg.303]    [Pg.378]    [Pg.25]    [Pg.684]    [Pg.88]    [Pg.621]    [Pg.118]    [Pg.213]    [Pg.460]    [Pg.87]    [Pg.966]    [Pg.1561]    [Pg.118]    [Pg.194]    [Pg.194]    [Pg.894]    [Pg.169]    [Pg.894]    [Pg.465]    [Pg.194]    [Pg.451]    [Pg.244]    [Pg.500]    [Pg.99]    [Pg.118]   
See also in sourсe #XX -- [ Pg.263 ]




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