The synthesis of dimethyl esters of dl-O,O'-dimethylfukiic acid and dl-O,O'-dimethylepifukiic acid.
نویسندگان
چکیده
منابع مشابه
histological evaluation of the effect of three medicaments; trichloracetic acid, formocresol and mineral trioxide aggregate on pulpotomized teeth of dogs
چکیده ندارد.
15 صفحه اولThe Stereochemical Configuration of DL-@-Fluoromalic Acid*
The synthesis of two isomers of nn-b-fluoromalic acid has been reported in a previous publication from this laboratory (1). On the basis of elementary analysis and equivalent weights, the two isomers were undoubtedly the threo and erythro isomers of nn-fi-fluoromalic acid. However, at that time it was not possible to make a definite assignment of stereochemical configuration to the two isomers....
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The Osiris system implements a data model which was originally conceived for view management in a database perspective. Although this data model was designed independently from the object-orientation and from the current of terminological logics, it present similarities with both but also important differences. This paper presents the main features of the Osiris system and its data model which ...
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Two experiments were conducted to evaluate the efficacy of dietary DL-methionine hydroxy analog-free acid (MHA-FA, 88%) compared with DL-methionine (DLM, 99%) as Met sources in pigs. In Exp. 1, a total of 245 crossbred pigs (initial BW of 6.4 kg [SD = 0.5]) were allotted to 7 treatments in 7 replicates for an experimental period of 28 d. The basal diet (BD) was formulated to contain 17.5% CP an...
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Abstract: New mono acid esters have been synthesized from the reaction of benzoic acid and mono-hydroxybenzoic acids with 2-phenoxyethanol separated from Urtica pilulifera, characterized, and screened for possible antioxidant, antifungal, antimicrobial and anticancer activities. These phenolic acid esters gave various degrees of free radical scavenging, but the values were lower than that of α-...
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ژورنال
عنوان ژورنال: Agricultural and Biological Chemistry
سال: 1975
ISSN: 0002-1369,1881-1280
DOI: 10.1271/bbb1961.39.2217