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Interaction of Two Prolamins with 1- 13 C Oleic Acid by 13 C NMR †

✍ Scribed by Forato, L. A.; Yushmanov, V. E.; Colnago, L. A.


Book ID
126206313
Publisher
American Chemical Society
Year
2004
Tongue
English
Weight
78 KB
Volume
43
Category
Article
ISSN
0006-2960

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📜 SIMILAR VOLUMES


Syntheses with stable isotopes: Oleic-1-
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## Abstract A synthesis of oleic‐1‐^13^C acid and its conversion to triolein‐1′,1″,1″′‐^13^C~3~ are described. 9‐Octadecynenitrile‐1‐^13^C was prepared from 1‐bromo‐8‐heptadecyne and sodium cyanide‐^13^C. Hydrolysis afforded stearolic‐1‐^13^C acid, which was reduced to oleic‐1‐^13^C acid by the act

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## Abstract The relative orientation of caffeine in stacks formed by self‐association in aqueous solution has been evaluated by both ^1^H‐ and ^13^C‐nmr spectroscopy. The data, which were interpreted through the calculation of ring‐current and atomic diamagnetic anisotropic effects of the caffeine