Die Stereochemie der fragmentierenden Enthalogenierung von 1??Chlor??1??fluor??2??(1??halogenalkyl) cyclopropanen
B Spahić, M Schlosser
Index: Spahic, Bojana; Schlosser, Manfred Helvetica Chimica Acta, 1980 , vol. 63, # 5 p. 1242 - 1256
Full Text: HTML
Citation Number: 10
Abstract
Summary A number of model substrates were submitted to zinc-promoted fragmentation, and the composition of the resulting mixture of isomeric fluorodienes was determined. The exocyclic reaction center, bearing the electrofugal leaving group, was found to undergo almost complete stereochemical randomization in the course of the reaction. On the other hand, the ring-opening proceeds stereoselectively. The rotation, which brings the ...
Related Articles:
[Lewis,E.S. et al. Journal of the American Chemical Society, 1968 , vol. 90, p. 662 - 668]
[Rowan, Daryl D.; Lane, Heather P.; Allen, John M.; Fielder, Simon; Hunt, Martin B. Journal of Agricultural and Food Chemistry, 1996 , vol. 44, # 10 p. 3276 - 3285]
[Lewis,E.S. et al. Journal of the American Chemical Society, 1968 , vol. 90, p. 662 - 668]