Kinetics of the epoxidation of geraniol and model systems by dimethyldioxirane
AL Baumstark, PJ Franklin, PC Vasquez, BS Crow
Index: Baumstark; Franklin; Vasquez; Crow Molecules, 2004 , vol. 9, # 3 p. 117 - 124
Full Text: HTML
Citation Number: 9
Abstract
Abstract: The mono-epoxidation of geraniol by dimethyldioxirane was carried out in various solvents. In all cases, the product ratios for the 2, 3 and 6, 7 mono-epoxides were in agreement with literature values. Kinetic studies were carried out at 23 ºC in the following dried solvent systems: acetone (k 2= 1.49 M-1 s-1), carbon tetrachloride/acetone (9/1, k 2= 2.19 M-1 s-1), and methanol/acetone (9/1, k 2= 17 M-1 s-1). Individual k 2 values were ...
Related Articles:
[Kamata, Keigo; Kotani, Miyuki; Yamaguchi, Kazuya; Hikichi, Shiro; Mizuno, Noritaka Chemistry - A European Journal, 2007 , vol. 13, # 2 p. 639 - 648]
[Adam, Waldemar; Peters, Karl; Renz, Michael Journal of Organic Chemistry, 1997 , vol. 62, # 10 p. 3183 - 3189]
[Zhang, Aiping; Li, Linqing; Li, Jun; Zhang, Yi; Gao, Shuang Catalysis Communications, 2011 , vol. 12, # 13 p. 1183 - 1187]