A synthesis of protoanemonin. The tautomerism of acetylacrylic acid and of penicillic acid
E Shaw
Index: Shaw Journal of the American Chemical Society, 1946 , vol. 68, p. 2510,2512
Full Text: HTML
Citation Number: 99
Abstract
Br Br Br the direction of the pseudo-acid maxima in the region 210-220 mp are characteristic of a, P-unsaturated lactones.* Apparently the ionic form of the acid is also derived from the cyclic structure since the aqueous solutions are strongly acidic and spectra of alkaline solutions show only a slight decrease of absorption at 220 mp III with production of a plateau in the region 270-290 rnp. Finally, the action of one iiiole of diazomethane on acetylacrylic ...
Related Articles:
[Srogl,J. Collection of Czechoslovak Chemical Communications, 1964 , vol. 29, p. 1380 - 1386]
[Bestmann,H.-J. et al. Justus Liebigs Annalen der Chemie, 1967 , vol. 706, p. 68 - 74]
[Bestmann,H.J. et al. Chemische Berichte, 1963 , vol. 96, p. 465 - 469]
[Srogl,J. Collection of Czechoslovak Chemical Communications, 1964 , vol. 29, p. 1380 - 1386]
[Kiehlmann,E. et al. Canadian Journal of Chemistry, 1976 , vol. 54, p. 1998 - 2003]