The friedel-crafts reaction of acid chlorides with ethene ; Di-addition and molecular rearrangement
作者:Francis X Bates、John A Donnelly、John R Keegan
DOI:10.1016/s0040-4020(01)80962-5
日期:1991.1
Acid chlorides, complexed with excess aluminiumchloride, reacted with ethene to form 3-methyl-2-buten-1-ones, i.e. rearranged di-addition products having a terminal isoprenoid skeleton, together with the usual β-chloropropanones. The latter were the sole products in the absence of excess catalyst. Acid chlorides containing a suitably situated π-system underwent intramolecular cyclization, e.g. 2-