Synthesis of Phenanthrenes. V. A Mechanism for the Cyclization of β-Arylethylcyclohexanols1
RA Barnes
Index: Barnes Journal of the American Chemical Society, 1953 , vol. 75, p. 3004,3007
Full Text: HTML
Citation Number: 16
Abstract
111, R= H IV, R= CH3 VIII, R CHI VII, R= H results in our own and other laboratories; however, Bromide I1 was rather unstable and hydrogen broit was difficult to formulate a mechanism which ex-mide was eliminated to some extent even during plained all the facts. vacuum distillation; however, satisfactory yields The purpose of this work was to study the cycli-of the desired alcohols could be obtained. zation of four new alcohols which were ...
Related Articles:
2, 3-Dihydrobenzofuran analogs of hallucinogenic phenethylamines
[Nichols; Snyder; Oberlender; Johnson; Huang Journal of Medicinal Chemistry, 1991 , vol. 34, # 1 p. 276 - 281]
High pressure nucleophilic fluoride-ion substitution reactions: formation of fluoroalkylbenzenes
[Gerdes, John M.; Keil, Robert N.; Shulgin, Alexander T.; Mathis, Chester A. Journal of Fluorine Chemistry, 1996 , vol. 78, # 2 p. 121 - 129]