Stephen B. Coan, and Dominick Papa. J. Am. Chem. Soc. , 1955, 77 (9), pp 2402â2404. DOI: 10.1021/ja01614a013. Publication Date: May 1955. ACS Legacy...
Received December 27,1960. Salts of lipoidal, ionic character were obtained by the selective reactions of 8-quinolinyl benzoate with certain salicylic acids.
Nov 4, 2006 - Antifungal Pisum satiVum Defensin 1 Interacts with Neurospora crassa Cyclin F. Related to the Cell Cycleâ . Denise S. Lobo,â¡,§ Iuri B. Pereira,â¡ ...
Apr 29, 2013 - from a Nasutitermes sp. Termite. Charlotte Nirma,. â ,â¡ ... demonstrates that social insects have evolved behavioral and physiological defense ...
Y.; Lee, B. M. Han'guk Nonghua Hakhoechi 2003, 46, 151. (9) (a) Grohe, K.; Frohberger, P. E.; Scheinpflug, H. DE 2248819, 1974. (b). Inayama, S.; Mamoto, K.; ...
Xing-Cong Li,â Hala N. ElSohly,â Alison C. Nimrod,â and Alice M. Clark*,â ,â¡. National Center for the Development of Natural Products, Research Institute of ...
Sep 16, 2010 - agent approved by the FDA, widely used in clinical practice and effective against a large spectrum of fungi, into silica nanoparticles.
and H-6â²(J2â²,3â²ax ) 14 Hz and J5â²ax,6â² ) 11 Hz), attribut- able to trans-diaxial interactions, served to identify protons in pseudo-axial positions (Figure 2).
May 26, 2014 - ABSTRACT: Antifungal resistance and toxicity problems of conventional fungicides highlighted the ... agricultural practice.7 Therefore, it is very important to control ... dimensional (2D) NMR data were recorded on a Varian Unity 500 .
displayed antimicrobial activity against 7 bacteria including Clostridium perfringens, Pseudomonas aeruginosa, and a hospital isolate of methicillin resistant ...
M. Iqbal Choudhary. H. E. J. Research Institute of Chemistry, University of Karachi, Karachi-75270, Pakistan, Department of Chemistry,. Cornell University, Ithaca ...
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STEPHEN B. COAN AND
was heated for 2-4 hours a t 100'. Any excess of unused amine and solvent was removed by evaporation in uucuo. The residue was basified with a small amount of cold 20% aqueous sodium hydroxide (to P H 11) and the precipitated solid bis-aminoamide was collected by suction and washed with a little cold water. The products were purified by recrystallization from ethyl acetate, hexane or mixtures of these solvents. Yields were usually above 90%.
[CONTRIBUTION FROM
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DOMINICK PAPA
Vol. 77
The bis-tertiary-aminoacetylamides were quaternized by refluxing with methyl iodide in methanol for several hours. The bis-methiodides crvstallized from meth ~ n o lor metlianol-ethyl
