An efficient chemomicrobiological synthesis of stable isotope-labeled L-tyrosine and L-phenylalanine
TE Walker, C Matheny, CB Storm…
Index: Walker, T. E.; Matheny, C.; Storm, C. B.; Hayden, H. Journal of Organic Chemistry, 1986 , vol. 51, # 8 p. 1175 - 1179
Full Text: HTML
Citation Number: 33
Abstract
7 a. 3'. 5*-'3c2 b. 4'-'3C proceeded smoothly. 10 Filtration into HC1 gave the protonated anilinium species, which is stable to air oxidation. An equivalent amount of NaNOz was added to the cold solution, and after 1 h an excess of hypophosphorous acid was added. The formation of phenol, as followed by 13C NMR, was complete after 4-5 days at room temperature. The phenol was isolated by ether extraction followed by codistillation with ...
Related Articles:
[Journal of the American Chemical Society, , vol. 120, # 28 p. 6851 - 6858]
[Seisser, Birgit; Zinkl, Rene; Gruber, Karl; Kaufmann, Franz; Hafner, Andreas; Kroutil, Wolfgang Advanced Synthesis and Catalysis, 2010 , vol. 352, # 4 p. 731 - 736]
Synthesis of 2-and 3-fluorotyrosine with dilute fluorine gas
[Journal of Fluorine Chemistry, , vol. 37, p. 267 - 278]
Synthesis of 2-and 3-fluorotyrosine with dilute fluorine gas
[Journal of Fluorine Chemistry, , vol. 37, p. 267 - 278]
Synthesis of 2-and 3-fluorotyrosine with dilute fluorine gas
[Journal of Fluorine Chemistry, , vol. 37, p. 267 - 278]