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Furyl acetamide

Eudy, L. W. Walla, M. D. Hudson, J. R. Morgan, S. L. Fox, A. Gas chromatog-raphy-mass spectrometry studies on the occurrence of acetamide, propionamide and furyl alchohol in pyrolysates of bacteria, bacteria fractions and model compounds. J. Anal. Appl. Pyrolysis 1985, 7, 231-247. [Pg.336]

Amides and sulfonamides undergo intramolecular chemistry to form aryl amides and aryl sulfonamides (Equations (17)—(19)) in the presence of palladium catalysts ligated by arylphos-phines.35,89 Initially, complexes of P(furyl)3 and P(o-tol)3 were most effective catalysts, but complexes of Hayashi s MOP and van Leeuwen s DPEphos and xantphos have lately been shown to be more active.90 In the presence of catalysts containing one of these ligand systems, five-, six-, and seven-membered rings were formed from halogenated benzamides or from substrates containing an acetamide, an A-carbobenzyloxy, or a t-butylcarbamate substituent tethered to the aryl halide (Equations (18) and (19)) ... [Pg.379]

SYNS 2-ACETAMINO-4-(5-NITRO-2-FURYI.)THIA-ZOLE 2-ACETYLAMIN0.4-(5-NITR0-2-FURYL)-THIAZOLE . N-(4-(5-NTTRO-2-FURANYL)-2-THIAZOLYL)ACETAMIDE N-(4-(5-NITRO-2-FURYL)-2-THIAZOLYL)ACETAMIDE N-(4-(5-NITRO-2-FURYL)THIAZOL-2-YL)ACETAMIDE... [Pg.3]

TRIFLUORO-N-(4-(5-NITRO-2-FURYL)-2-THIAZOLYL)ACETAMIDE see NGN500 a,a,a-TRIFLUORO-m-NITROTOLUENE see NFJ500 TRIFLUOROPERAZINE DIHYDROCHLORIDE see TKK250... [Pg.1921]

Diazines. - Like phenylglyoxal, 2-furylglyoxal condenses with amino-acetamide to give a 5-arylpyrazin-2-one (127) (28%) chlorination of this material, followed by phase-transfer-catalysed oxidation of the furyl group, affords the carboxylic acid (128) (Scheme 66). ... [Pg.322]

Nitrofurfurylidene)-amino]-2-imidazolidinone N-[4-(5-Nitro-2-furyl)-2-thiazolyl]acetamide Nitrogen mustard (Mechlorethamine)... [Pg.236]

Amino-5-(5-nitro-2-furyl)-l, 3,4-thiadiazole A -[5-(5-Nitro-2-furyl)-l, 3,4-thiadiazol-2-yl]-acetamide... [Pg.400]

Mattammal, M. B., T. V. Zenser, M. O. Palmier, and B. B. Davis. 1985. Renal reduced nicotinamide adenine dinucleotide phosphate cytochrome c reductase-mediated metabolism of the carcinogen V-[4-(5-nitro-2-furyl)-2-thiazolyl]acetamide. Cancer Res. 45 149-156. [Pg.113]

See other pages where Furyl acetamide is mentioned: [Pg.202]    [Pg.457]    [Pg.457]    [Pg.202]    [Pg.457]    [Pg.457]    [Pg.102]    [Pg.131]    [Pg.1575]    [Pg.49]    [Pg.221]    [Pg.130]    [Pg.1806]    [Pg.499]    [Pg.925]    [Pg.305]    [Pg.388]   


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