Apr 27, 2018 - Me. 165-166. 58 c'.oH.oXCl c ,. H, X. A s. 10. III. II. H. Et. 180-180.5. 57 c'nlluXCi c ,. II, x,¡. A s. .... 3'-methy i-o-hydroxy-tu...
acetoxycoumarinir acid,4 there x-as added 9.3 g (0.1 mole) of. C6H:,SH$ at room .... for work, and the C.S.I.R., Sew Delhi, for a junior. Research Fellowship (to ...
Richard S. Hutton, Heinz D. Roth,* Marcia L. Manion Schilling, and J. William Suggs. Contribution from Bell Laboratories, Murray Hill, New Jersey 07974.
Preparation and Geometric Isomerism of Dipiperonylidenesuccinic Acid and Anhydride. D. P. Chakraborty, Thomas Sleigh, Robert Stevenson, Gertrude A.
G. O. Burr. Linolenic acid having an essentially theoretical iodine value may be prepared only by the de- bromination of the ether-insoluble alpha-hexa-.
Nov 27, 2007 - Citation data is made available by participants in Crossref's Cited-by Linking service. For a more comprehensive list of ... Synthesis of o-Carboxyarylacrylic Acids by Room Temperature Oxidative Cleavage of Hydroxynaphthalenes and High
Nov 27, 2007 - A structureâantifungal activity relationship (SAR) study of 22 related cinnamic acid derivatives was carried out. Attention was focused on the antifungal activities exhibited against Aspergillus flavus, Aspergillus terreus, and Asper
Mar 9, 1981 - Soc. 1981, 103, 5147-5151. 5147. Geometric Isomerism in Quinolylmethylenes. Richard S. Hutton, Heinz D. Roth,* Marcia L. Manion Schilling, ...
Dec 29, 2008 - Phone: +34 963864879(E.G.-E.). Fax: +34 963864322 (E.G.-E.)., â ... is made available by participants in Crossref's Cited-by Linking service.
There is a report that five-membered .... In 1960 Reutov and Lovtsova1 reported a useful syn- .... Simmons, Jr., A. J.-H. Treiber, and S. R. Dowd, J. Am. Chem.
Per for 30 hr. \\.ork-iip i i i the iisua1 maiirier gave 3 1 . i g of the free haw. Treatment of the baqe with HC1 gas i i i E120 gave H solid which iva* recpstd (?ile?CO).
Antifungal Activity and Geometric Isomerisni. Anilides of o-Coumarinic Acid
The report by Schultz' that ariilides of o-coumaric acid poqvsaed some antifungal propertiei prompted the preparation of
