The Preparation of 3,4,5-d3-Lithocholic Acid. W. H. Pearlman, M. R. J. Pearlman, S. Elsey. J. Am. Chem. Soc. , 1949, 71 (12), pp 4126â4127. DOI: 10...
uble hydrolytic fraction could not be obtained in crystalline form. It proved to have a neutral equivalent of about 360 and yielded two moles of.
Preparation of 3- and 4- (4-nitrophenyl)phthalic acid. Olden E. Paris. J. Chem. Eng. Data , 1970, 15 (3), pp 459â461. DOI: 10.1021/je60046a032. Publication ...
Sterling-Winthrop. Research Institute]. The Preparation of 3-Halo-4-dialkylaminoalkylaminoquinoline Derivatives. By Alexander R. Surrey and Royal A. Cutler.
tion of the general methods used by us is given here. ... very satisfactory for this purpose. The mass is ... In a bomb of a high-pressure hydrogenator, 200.
DOI: 10.1021/ja01853a032. Publication Date: August 1941. ACS Legacy Archive. Cite this:J. Am. Chem. Soc. 1941, 63, 8, 2137-2138. Note: In lieu of an abstract ...
Publication Date: December 1950. ACS Legacy Archive. Cite this:J. Am. Chem. Soc. 72, 12, 5760-5761. Note: In lieu of an abstract, this is the article's first page.
May 1, 2002 - Pooran Chand, Yarlagadda S. Babu, Shanta Bantia, Naiming Chu, L. Brent Cole, Pravin L. Kotian, W. Graeme Laver, John A. Montgomery, Ved ...
[Contribution from the Chemical Laboratory of the University of Kansas] ... By F. B. Dains, R. Q. Brewster, I. L. Malm, A. W. Miller, R. V. Maneval and.
Mrs. Rosita B. Feliu for valuable technical assistance. The Preparation of 4-Pentenenitriles and 3,4-Pentadienenitriles from. N-(2-Alkenyl)- and N-(2-Alkynyl) ...
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W. H. PEARLMAN, M. R. J. PEARLMAN AND S. ELSEY
Vol. 71
uble hydrolytic fraction could not be obtained in the type of sugar linkages involved (a or p) was crystalline form. It proved to have a neutral obtained. equivalent of about 360 and yielded two moles of Summary B-hydroxydecanoic acid upon saponification. As no such ester is formed by the conditions employed A crystalline, acidic glyco-lipide was produced during hydrolysis, and as H the proportion of this I compound decreases with C-O-CH-CHp-COO-CH-CH1-COOH concluded hydrolysis that time, twoitmoles was [
