The Ritter Reaction of Tertiary Trihalomethylcarbinols and Related Substances
A Kaluszyner, S Blum…
Index: Kaluszyner,A. et al. Journal of Organic Chemistry, 1963 , vol. 28, p. 3588 - 3590
Full Text: HTML
Citation Number: 8
Abstract
Then a plot of kinst us. k,nst [Cl-] should yield a straight line of slope k2/k3 and y-intercept k,. Instantaneous rate constants ob- tained from the slope of the curved "first-order" plots at several points were treated in this manner. Method B.-The substitution [Cl-] = c + r - [RCl] is made in eq. 2, where c is chloride concentration at a time taken as t = 0 and T is the concentration of substrate at t = 0. This equation may now be integrated to yield, after rearrangement
Related Articles:
[Thomas, Richard R.; Chebolu, Venkatasuryanarayana; Sen, Ayusman Journal of the American Chemical Society, 1986 , vol. 108, # 14 p. 4096 - 4103]
Reductive alkylation/arylation of arylcarbinols and ketones with organosilicon compounds
[Cella, J. A. Journal of Organic Chemistry, 1982 , vol. 47, # 11 p. 2125 - 2130]
Reactions of trimethylsilyl-derived iodohydrins with electron-rich π-systems
[Ishai, Eti; Shamai, Sarit; Feit, Ben-Ami Journal of the Chemical Society. Perkin Transactions 1, 2002 , # 3 p. 434 - 438]
Reductive alkylation/arylation of arylcarbinols and ketones with organosilicon compounds
[Cella, J. A. Journal of Organic Chemistry, 1982 , vol. 47, # 11 p. 2125 - 2130]
[Basavaiah, Deevi; Reddy, Kanumuri Ramesh Organic Letters, 2007 , vol. 9, # 1 p. 57 - 60]