scholarly journals Purification and characterization of bovine parotid hypocalcemic factor obtained via extraction with glacial acetic acid.

1978 ◽  
Vol 26 (7) ◽  
pp. 1957-1965 ◽  
Author(s):  
AKIRA MIZUTANI ◽  
IKUKATSU SUZUKI ◽  
HAJIMU YAMAMOTO
2016 ◽  
Vol 13 (2) ◽  
pp. 244-252
Author(s):  
Baghdad Science Journal

In this paper, some chalcone derivatives (C1, C2) were synthesized based on the reaction of equal amount of substituted acetophenone and substituted banzaldehyde in basic medium. Oxazine and thiazine derivatives were prepared from the reaction of chalcones (C1-C2) with urea and thiourea respectively in a basic medium. Pyrazole derivatives were prepared based on the reaction of chalcones with hydrazine mono hydrate or phenyl hydrazine in the presence of glacial acetic acid as a catalyst. The new synthesized compounds were identified using various physical techniques like1 H-NMR and FT-IR spectra.


1969 ◽  
Vol 52 (5) ◽  
pp. 1100-1105
Author(s):  
W P Cochrane

Abstract The effect of strong basic reagents on the title compounds was investigated. The dehydrochlorination of cis-chlordane proceeds rapidly to give 3-chlorochlordene, whereas its isomer, trans-chlordane, loses HCl very slowly to yield 2-chlorochlordene. The difference in rates of HCl elimination and the formation of isomeric chloro-vinyl derivatives is discussed with reference to the mechanisms of the reactions and the structures of the parent compounds. The action of basic reagents on heptachlor epoxide resulted in preferential epoxide isomerization (or rearrangement) to an allylic alcohol derivative. The structure of this α,β- unsaturated alcohol was elucidated from the characterization of the products formed by chlorination and oxidation. Ileptachlor undergoes substitution to give 1-hydroxychlordene in basic hydroxylic media. The addition reactions of tert.-butyl hypochlorite/glacial acetic acid to both heptachlor and aldrin are also mentioned.


e-Polymers ◽  
2009 ◽  
Vol 9 (1) ◽  
Author(s):  
Abdol Reza Hajipour ◽  
Parniyan Roosta ◽  
Saeed Zahmatkesh ◽  
Arnold E. Ruoho

Abstract N,N´-(3,3´,4,4´-Benzophenonetetracarboxylic)-3,3´,4,4´-diimido-di-Lamino acids (1a-1d) and N,N´-pyromelliticdiimido-di-L-amino acids (2a-2d) are prepared from the reaction of 3,3´,4,4´-benzenetetracarboxylic-3,3´,4,4´- dianhydride or pyromellitic dianhydride with the corresponding L-amino acids in a solution of glacial acetic acid/pyridine (3:2) at refluxing temperature. 4-(4-((4- Hydroxyphenylimino)methyl)benzylidene amino) phenol (3) is prepared from 4- amino phenol and terephthaldialdehyde in refluxing ethanol. Interfacial polycondensation method was used to prepare the corresponding polymers (PEII1-8) in two immiscible solvents (water/dichloromethane). The resulting poly(esterimide- imine)s (PEIIs) having good inherent viscosities (0.13-1.25 dl g-1), optical activity and thermal stabilities is obtained in high yields.


ACS Omega ◽  
2020 ◽  
Vol 5 (12) ◽  
pp. 6389-6394
Author(s):  
Yingjie Zhang ◽  
Guanqun Gong ◽  
Honglei Zheng ◽  
Xin Yuan ◽  
Liangwei Xu

2015 ◽  
Vol 52 (10) ◽  
pp. 6615-6622 ◽  
Author(s):  
Andri Cahyo Kumoro ◽  
Rizka Amalia ◽  
Catarina Sri Budiyati ◽  
Diah Susetyo Retnowati ◽  
Ratnawati Ratnawati

1955 ◽  
Vol 33 (4) ◽  
pp. 711-715 ◽  
Author(s):  
J. L. Barnwell ◽  
W. A. Saunders ◽  
R. W. Watson

Phosphorylation of 1,2-O-isopropylidene-D-xylose with diphenylphosphoro-chloridate yielded crystalline 1,2-O-isopropylidene-D-xylofuranose-5-diphenyl-phosphate. Subsequent hydrogenolysis in glacial acetic acid over Adams' catalyst quantitatively removed phenyl groups as shown by infrared analysis. Mild hydrolysis in acetic acid for two hours at 80 °C. removed the isopropylidene grouping, and D-xylose-5-phosphate was isolated as an amorphous barium salt. A yield of 81% of theoretical was obtained from 1,2-O-isopropylidene-D-xylose, or an over-all yield of 72% from xylose. The product was characterized through its amorphous barium, disodium, and dipotassium salts, and its crystalline dibrucine and distrychnine salts.


2003 ◽  
Vol 15 (21) ◽  
pp. 1699-1706
Author(s):  
Giaan A. Álvarez Romero ◽  
Alberto Rojas Hernández ◽  
Ma. Teresa Ramírez Silva ◽  
Mario A. Romero Romo ◽  
Pablo Rogelio Hernández

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