Abstract:
An acylated diketonic compound is produced by rearrangement of the corresponding enol ester in the presence of a cyanide source. In one embodiment the cyanide source is employed with a molar excess of a moderate base, with respect to the enol ester. In another embodiment, the cyanide source is a stoichiometric amount, with respect to the enol ester, of potassium or lithium cyanide and a catalytic amount of a Crown ether is used.
Abstract:
An acylated diketonic compound is produced by rearrangement of the corresponding enol ester in the presence of a cyanide source. In one embodiment the cyanide source is employed with a molar excess of a moderate base, with respect to the enol ester. In another embodiment, the cyanide source is a stoichiometric amount, with respect to the enol ester, of potassium or lithium cyanide and a catalytic amount of a Crown ether is used.
Abstract:
As new compounds, acyiaminoaryloxy and arylthio pyrimidines having the formula wherein A is oxygen or sulfur; M is CH or N; X is hydrogen, lower alkyl, halo, methoxy, alkoxy, C,-C 3 alkylthio, cyano, carbomethoxy or trifluoromethyl; Z is
wherein R' is C 1 -C 8 straight, branched-chain or halo-alkyl, aryl; and R is hydrogen, C 1 -C 8 straight or branched chain alkyl, C 5 or C 6 cycloalkyl or ary
Abstract:
As new compounds, acyiaminoaryloxy and arylthio pyrimidines having the formula wherein A is oxygen or sulfur; M is CH or N; X is hydrogen, lower alkyl, halo, methoxy, alkoxy, C,-C 3 alkylthio, cyano, carbomethoxy or trifluoromethyl; Z is wherein R' is C 1 -C 8 straight, branched-chain or halo-alkyl, aryl; and R is hydrogen, C 1 -C 8 straight or branched chain alkyl, C 5 or C 6 cycloalkyl or ary