The Lithium Aluminum Hydride Reduction of p-Substituted Stilbene Oxides
A Feldstein, CA VanderWerf
Index: Feldstein; VanderWerf Journal of the American Chemical Society, 1954 , vol. 76, p. 1626,1627
Full Text: HTML
Citation Number: 23
Abstract
As part of a study of the effect of electronic factors on the direction of sN2 ring opening in unsymmetrical epoxides where steric factors are largely eliminated, the reduction of trans-p- methylstilbene oxide and trans-p-chlorostilbene oxide with lithium aluminun~ hvdride was investigated. trans-p-Methylstilbene oxide gave approximately 6Oy~ of p- methylbenzylphenylcarbinol and 407: of benzyl-p-tolylcarbinol, whereas trans-p- ...
Related Articles:
[Yamato, Takehiko; Hu, Jian-Yong; Shinoda, Naoki Journal of Chemical Research, 2007 , # 11 p. 641 - 643]
[Cella, James A.; Bacon, Sidney W. Journal of Organic Chemistry, 1984 , vol. 49, p. 1122 - 1125]
[Yamato, Takehiko; Hideshima, Chieko; Prakash, G. K. Surya; Olah, George A. Journal of Organic Chemistry, 1991 , vol. 56, # 6 p. 2089 - 2091]
[Yamato, Takehiko; Hu, Jian-Yong; Shinoda, Naoki Journal of Chemical Research, 2007 , # 11 p. 641 - 643]
[Bach, Peter; Albright, Andrea; Laali, Kenneth K. European Journal of Organic Chemistry, 2009 , # 12 p. 1961 - 1966]