نتایج جستجو برای: aryl amides

تعداد نتایج: 18345  

Journal: :Environmental Health Perspectives 1983
D. Malejka-Giganti C. L. Ritter C. N. Ryzewski

Metabolic or synthetic N-hydroxylation of N-arylamides yields N-arylacylhydroxamic acids considerably more carcinogenic for the rat mammary gland than the parent amides both by systemic and topical administration. The size of the aryl moiety, the position of the nitrogen relative to the aryl moiety and the type of acyl group are determinants of the carcinogenic potency of N-arylacylhydroxamic a...

Journal: :Journal of chromatographic science 2009
Tarek Belal Tamer Awad C Randall Clark Jack DeRuiter

A series of acylated derivatives of 3,4-methylenedioxy-methamphetamine (3,4-MDMA) are prepared and evaluated in gas chromatography-mass spectrometry (GC-MS) studies. The perfluoroalkyl amides of 3,4-MDMA show the lowest GC retention, while the aromatic amides such as the benzamide show the greatest retention on the dimethylpolysiloxane stationary phase (Rtx-1). The mass spectral properties of t...

2013
Bernd Wrackmeyer Jürgen Weidinger

Ever since their first synthesis in 1974 monomeric tin(II) and lead(II) amides have attracted con­ siderable interest as a consequence of their carbenoid electronic structure [1 6]. Although the sub­ stituents at the nitrogen atoms have been varied to some extent, N-dialkylboryl groups have received only scant attention. One attempt to use a N-dimethylboryl group has afforded a dimer after elim...

Aziz Shahrisa Salar Hemmati

Synthesis of 4-(N,N- dimethylamino)-3-aryl-3-butene-2-one, ethyl-5-aryl-4-oxo-4H-pyran-2-carboxylate, ethyl-5-aryl-4-pyridones-2-carboxylate and 5-aryl-3-cyano-5-methyl-2-pyridones (aryl=3-thienyl, 2-furyl) are described.

Journal: :Molecules 2016
Joo Tae Hwang Yesol Kim Hyun-Jae Jang Hyun-Mee Oh Chi-Hwan Lim Seung Woong Lee Mun-Chual Rho

Two new feruloyl amides, N-cis-hibiscusamide (5) and (7'S)-N-cis-feruloylnormetanephrine (9), and eight known feruloyl amides were isolated from Portulaca oleracea L. and the geometric conversion of the ten isolated feruloyl amides by UV light was verified. The structures of the feruloyl amides were determined based on spectroscopic data and comparison with literature data. The NMR data reveale...

Journal: :The Biochemical journal 1950
H G BRAY S P JAMES J W V THORPE M R WASDELL

Studies of the amidase activity ofextracts of various animal tissues have been reported in earlier papers (Bray, James, Ryman & Thorpe, 1948; Bray, James, Raffan, Ryman & Thorpe, 1949a; Bray, Thorpe & Wood, 1949c; Bray, James, Thorpe, Wasdell & Wood, 1949 b). The present paper records further observations, including the behaviour of the enzyme towards some saturated long-chain and w-phenylsubst...

Fe3O4 nanoparticles were employment as an efficient and magnetically separable Nano catalyst for the synthesis of amides via one-pot Beckmann rearrangement of ketones under solvent-free conditions. Various secondary amides were synthesized by this method in moderate to good yields. The catalyst showed high thermal stability and was recovered and reused at least five times without any considerab...

پایان نامه :دانشگاه آزاد اسلامی - دانشگاه آزاد اسلامی واحد یزد - دانشکده شیمی 1393

واکنش های تک ظرفی دو مینو، آریل آمین ها، آلکیل پروپیولات ها، ایزاتین و ایندول در حلال اتانول و در دمای اتاق با استفاده از fecl3 به عنوان کاتالیزور مورد بررسی قرار گرفت، که منجر به تشکیل محصول 2-(2-oxo-1,2-dihydro-1h-[3,3]biindolyl-3-yl)-3-aryl amine-acrylic acid alkyl ester با راندمان بالا گردید.

Journal: :Chemical communications 2013
Michael S Perryman Matthew E Harris Jade L Foster Anushka Joshi Guy J Clarkson David J Fox

Amino-amides are important pharmaceutical building-blocks. The enantioselective reduction of trichloromethyl ketones using ruthenium transfer hydrogenation catalysts is reported. The products react in a range of Jocic-type reactions to give enantiomerically enriched amino-amides.

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