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Ethylenecarboxylic acid amides

Amino-a,j5-ethylenecarboxylic acid amides from a-trichloroacetylketones... [Pg.391]

N-Bromosuccinimide I sodium hydride I dimethy Iformamide 4-a-Bromo-2-azetidinones from p,y-ethylenecarboxylic acid amides... [Pg.98]

Fallacious acetatej 1,3-bis(diphenylphosphino)propane (E)-p,y-Ethylenecarboxylic acid amides from 2-ethyleneamines Carbonylation... [Pg.130]

Y,6-Ethylenecarboxylic acid amides from O-allyliminoesters Thermal [3.3)-sigmatropic rearrangement... [Pg.143]

Syntheses with a-(arylsulfonylmethyl)-a,p-ethylenecarboxylic acid amides <-... [Pg.174]

Methylene-2-azetidinones from p-bromo-p,Y-ethylenecarboxylic acid amides Modified Ullmann-Goldberg reaction... [Pg.375]

Asym. diene synthesis with a,p-ethylenecarboxylic acid amides Effect of Lewis acid on the sense of asym. induction... [Pg.419]

A soln. of startg. a-chloroketimine in THF added to a soln of /-Pr2NLi in the same solvent at 0°, after 2 h acetone added dropwise, and stirring continued for 10 h with warming to room temp. - product. Y 80%. This is part of a 2-step synthesis of a,P-oxidoketones which cannot be obtained directly by the Darzens-Claisen route with diaryl ketones, P,y-ethylenecarboxylic acid amides were obtained with excess i-PrjNLi, especially in the presence of HMPA. F.e.s. P. Sulmon et al., J. Org. Chem. 53, 4457-62 (1988). [Pg.446]

See other pages where Ethylenecarboxylic acid amides is mentioned: [Pg.160]    [Pg.475]    [Pg.103]    [Pg.180]    [Pg.182]    [Pg.94]    [Pg.189]    [Pg.249]    [Pg.415]    [Pg.187]    [Pg.204]    [Pg.237]    [Pg.269]    [Pg.269]    [Pg.270]    [Pg.270]    [Pg.290]    [Pg.299]    [Pg.438]    [Pg.530]    [Pg.536]    [Pg.178]    [Pg.185]    [Pg.212]    [Pg.218]    [Pg.224]    [Pg.230]    [Pg.312]   


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A,p Ethylenecarboxylic acid amide

A,£-Ethylenecarboxylic acid amides

Ethylenecarboxylic acid

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