Substituent effects on the solvolysis rates and gas phase stabilities of 1,2,2-trimethyl-1-phenylpropyl and 1,2,2-trimethyl-1-(2-methylphenyl)propyl systems
Substituent effects on the solvolysis rates of 1,2,2-trimethyl-1- phenylpropyl chlorides in 80% (v/v) aq acetone at 45 °C and 1,2,2-trimethyl- 1-(2-methylphenyl)propyl p-nitrobenzoates in 50% (v/v) aq ethanol at 75 °C were correlated with the Yukawa-Tsuno
Substituent-induced chemical shifts in 3- and 4-substituted styrenes: factor analysis of the styrene data matrix
The techniques of factor analysis are used to investigate a data matrix constructed from magnetic resonance parameters for seventy-five 4-substituted styrenes, α-methylstyrenes, and α-tert-butylstyrenes and 3-substituted styrenes and α-methylstyrenes (wit
Reynolds, William F.,Gomes, Anabela,Maron, Antonina,MacIntyre, Douglas W.,Maunder, Robert G.,et al.
p. 2367 - 2375
(2007/10/02)
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