SELECTIVITY IN THE SYNTHESIS OF FLUORINATED HETEROCYCLES FROM ALPHA,BETA-UNSATURATED PERFLUOROACYL DERIVATIVES (OR THEIR SYNTHETIC EQUIVALENTS) AND 1,2-BIS-NUCLEOPHILES
B. Dondy et al., SELECTIVITY IN THE SYNTHESIS OF FLUORINATED HETEROCYCLES FROM ALPHA,BETA-UNSATURATED PERFLUOROACYL DERIVATIVES (OR THEIR SYNTHETIC EQUIVALENTS) AND 1,2-BIS-NUCLEOPHILES, Tetrahedron letters, 35(25), 1994, pp. 4357-4360
Reactions of vicinal diamines, aminoalcohols, aminothiols with synthet
ic equivalents of perfluoroenones 3 or alpha,beta-unsaturated perfluor
oesters 6 gave regiospecifically new five member (imidazo or oxazolidi
nes) or seven member fluorinated heterocycles (dia or thiazepines).