Regioselektive Metallierung des Phenylcyclopropans sowie leichte Anlagerung des 1??Phenylcyclopropyl??kaliums an Äthylen
M Schlosser, P Schneider
Index: Schlosser, Manfred; Schneider, Philippe Helvetica Chimica Acta, 1980 , vol. 63, # 8 p. 2404 - 2410
Full Text: HTML
Citation Number: 20
Abstract
Summary Whereas pentyl sodium in pentane mainly promotes a hydrogedmetal exchange reaction at the m-and p-position of phenylcyclopropane, both the butyllithiuml potassium t- butoxide reagent and trimethylsilylmethyl potassium in tetrahydrofuran convert phenylcyclopropane exclusively into 1-phenylcyclopropyl potassium. The latter organometallic derivative adds smoothly onto the double bond of ethylene at ...
Related Articles:
[Soderquist, John A.; Huertas, Ramon; Leon-Colon, Gisela Tetrahedron Letters, 2000 , vol. 41, # 22 p. 4251 - 4255]
[Ogle, Craig A.; Black, Kristyna C.; Sims, Philip F. Journal of Organic Chemistry, 1992 , vol. 57, # 12 p. 3499 - 3503]
[Ouellette,R.J. et al. Journal of the American Chemical Society, 1968 , vol. 90, p. 1619 - 1624]
[Ouellette,R.J. et al. Journal of the American Chemical Society, 1968 , vol. 90, p. 1619 - 1624]
[Ouellette,R.J. et al. Journal of the American Chemical Society, 1968 , vol. 90, p. 1619 - 1624]