Cyclic hydroboration of 1, 5-cyclooctadiene. A simple synthesis of 9-borabicyclo [3.3. 1] nonane, an unusually stable dialkylborane
EF Knights, HC Brown
Index: Knights, E. F.; Brown, H. C. Journal of the American Chemical Society, 1968 , vol. 90, p. 5280 - 5281
Full Text: HTML
Citation Number: 92
Abstract
-5910",[@ IzE6-9350",[@] 278-9700"(c 0.270, dioxane). Thus the specimen of hydrindanone produced from the octalin contained 92 9 and 8 of its enantiomer which, in turn, represented the composition of the octalones 4b and 4a, respectively. The enantiomeric ratios of various octalone specimens thus were calculated from their ORD curves using the established value,[@ I222+ 11, 150", for the pure enantiomer 4b. The asymmetric induction observed ...
Related Articles:
[Soderquist, John A.; Brown, Herbert C. Journal of Organic Chemistry, 1980 , vol. 45, # 18 p. 3571 - 3578]
[Knights,E.F.; Brown,H.C. Journal of the American Chemical Society, 1968 , vol. 90, p. 5283 - 5284]
Oxidation of ketals to orthocarbonates: a double Baeyer-Villiger reaction
[Bailey, William F.; Shih, Mei-Jue Journal of the American Chemical Society, 1982 , vol. 104, # 6 p. 1769 - 1771]
[Soderquist, John A.; Colberg, Juan C.; Valle, Luis Del Journal of the American Chemical Society, 1989 , vol. 111, # 13 p. 4873 - 4878]
[Soderquist, John A.; Colberg, Juan C.; Valle, Luis Del Journal of the American Chemical Society, 1989 , vol. 111, # 13 p. 4873 - 4878]