79803-42-2Relevant academic research and scientific papers
On the Stereochemistry of Diaryl-Substituted Cyclohexanones Formed by Michael Reactions. Trans to Cis Isomerization of Their Ketals under Basic Conditions
Rowland, Alex T.,Filla, Sandra A.,Coutlangus, Marilyn L.,Winemiller, Mark D.,Chamberlin, Mark J.,Czulada, Gary,Johnson, Steven D.,Sabat, Michal
, p. 4359 - 4365 (2007/10/03)
The stereochemistry of C-1-substituted 2,6-diphenylcyclohexan-4-ones 1-3 prepared by Michael reactions has been investigated. While preparations of these compounds have been reported over the past 70 years, in many instances the correct stereochemistry at
Saponification of Dimethyl cis-2,6-Diphenyl-4-oxocyclohexane-1,1-dicarboxylate. A Reinvestigation
Rowland, Alex T.,Hohneker, John A.,McDaniel, Keith F.,Moore, David S.
, p. 301 - 306 (2007/10/02)
The saponification of dimethyl cis-2,6-diphenyl-4-oxocyclohexane-1,1-dicarboxylate was reported over 50 years ago to produce the corresponding diacid.The ease with which the reaction occurred is surprising considering the steric factors involved.We have f
