Structural effects in solvolytic reactions. 50. Steric retardation in the solvolysis of tertiary endo bicyclic derivatives. Evidence that the exo:endo rate/product ratios for typical reactions in rigid U-shaped bicyclics is a general steric phenomenon
Rates of solvolysis of the p-nitrobenzoates of the tertiary 2-methyl- and 3-methyl-cis-bicyclo[3.3.0]octanols. Evidence for steric hindrance to ionization in the endo derivatives
作者:Herbert Charles. Brown、Walton J. Hammar
DOI:10.1021/ja01000a084
日期:1967.11
BROWN, H. C.;JAGT, D. L. V.;ROTHBERG, I.;HAMMAR, W. J.;KAWAKAMI, J. H., J. ORG. CHEM., 1985, 50, N 12, 2179-2188
作者:BROWN, H. C.、JAGT, D. L. V.、ROTHBERG, I.、HAMMAR, W. J.、KAWAKAMI, J. H.