Chemical and Pharmaceutical Bulletin p. 734 - 737 (1995)
Update date:2022-08-31
Topics:
Ozaki
Kubo
Okamura
Kim
A new procedure using lithium chloride in hexamethylphosphoramide was found to be useful for the synthesis of Michael-type adducts and cyclic enones. Selectivity for the two products could be controlled by altering the reaction temperature employed. The urea-type solvents were also examined instead of hexamethylphosphoramide.
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