Cyclohexane compounds. VII. Nucleophilic scission of the stereoisomeric 3-methoxycyclohexene oxides
作者:R. A. B. Bannard、A. A. Casselman、E. J. Langstaff、R. Y. Moir
DOI:10.1139/v68-006
日期:1968.1.1
trans-3-methoxycyclohexene oxides by hydrogen chloride, hydrogen bromide, ammonia, acetic acid, and methanol (under both acidic and alkaline conditions) has been examined using vapor-phase chromatography to detect and isolate minor isomers. Approximately 10% of the product from opening of the trans oxide is formed by attack at position-2 with each of these nucleophiles, whereas opening of the cis oxide proceeds exclusively
The configurations of the 3-Methoxycyclohexene Oxides. A Novel Application of Proton Magnetic Resonance Spectroscopy to the Determination of Structure and Configuration<sup>1</sup>