Hydroboration. XIII. The hydroboration of dienes with disiamylborane. A convenient procedure for the conversion of selected dienes into unsaturated alcohols
G Zweifel, K Nagase, HC Brown
文献索引:Zweifel,G. et al. Journal of the American Chemical Society, 1962 , vol. 84, p. 190 - 195
Whereas the dihydroboration of 1.3-butadiene with diborane results in major amounts of addition of the boron at the internal position, producing after oxidation 24-357'of the 1, 3- butanediol, dihydroboration with disiamylborane achieves a more selective conversion of the diene into the terminal derivative, 10 Yo 1, 3-and 907'1, 4-butanediol. Dihydroboration of 1, 4-pentadiene yields a 15: 85 distribution of 1, 4-and 1, 5-pentanediol, whereas the ...
[Ager, David J.; Anderson, Ken; Oblinger, Eric; Shi, Yian; Vanderroest, James Organic Process Research and Development, 2007 , vol. 11, # 1 p. 44 - 51]