作者:Yu.S. Shabarov、L.D. Sychkova、S.G. Bandaev
DOI:10.1016/s0022-328x(00)88450-8
日期:1975.10
Mercuration of trans-1-phenyl-2-cyclohexylcyclopropane and stereoisomeric 1,2-di- and 1,2,3-triphenylcyclopropanes has been studied. An increase in the number of substituents in the cyclopropane ring leads to an increase in the stability of the ring towards mercury acetate, and substitution in the aromatic ring is the main process with 1,2,3-triphenylcyclopropane.
研究了反式-1-苯基-2-环己基环丙烷和立体异构体的1,2-二-和1,2,3-三苯基环丙烷的汞化。环丙烷环中取代基数目的增加导致该环对乙酸汞的稳定性增加,芳环中的取代是1,2,3-三苯基环丙烷的主要过程。