Journal of the American Chemical Society

Reactions of Tricyclopropylcarbinol Derivatives

H Hart, PA Law

Index: Hart,H.; Law,P.A. Journal of the American Chemical Society, 1962 , vol. 84, p. 2462 - 2463

Full Text: HTML

Citation Number: 16

Abstract

Some time ago we reported3 that a second cyclopropyl group was nearly as effective as the first in accelerating the solvolysis of cyclopropylcarbinyl derivatives. Thus, the ratios of the solvolysis rates Io: 11: I2 (X= p-nitrobenzoate) in 80% aqueous dioxane at GOO were 1: 246: 23,500.? it the time, we were unsuccessful in attempts to

Related Articles:

Efficient Brønsted Acid Catalyzed Hydrations and Hydroaminations of (Dicyclopropylmethylene) cyclopropane

[Ackermann, Lutz; Kozhushkov, Sergei I.; Yufit, Dmitry S.; Marek, Ilan Synlett, 2011 , # 11 p. 1515 - 1518]

Ruthenium??Catalyzed Hydroarylation of Methylenecyclopropanes through C H Bond Cleavage: Scope and Mechanism

[Ackermann, Lutz; Kozhushkov, Sergei I.; Yufit, Dmitry S. Chemistry - A European Journal, 2012 , vol. 18, # 38 p. 12068 - 12077]

Stable Carbonium Ions. XVII. 1a Cyclopropyl Carbonium Ions and Protonated Cyclopropyl Ketones

[Pittman,C.U.; Olah,G.A. Journal of the American Chemical Society, 1965 , vol. 87, # 22 p. 5123 - 5132]

More Articles...