Synthesis, Separation of Tautomers and Biological Activities of 4,6-Diaryl-3-oxo-3,3a,4,5-tetrahydro-2H-indazoles
Three chalcones (1a, 1b and 1c) having phloroglucinol oxygenation pattern in ring-A have been converted into the corresponding 3,5-diaryl-6-carbethoxycyclohex-2-en-1-ones (2a, 2b and 2c) by the Michael condensation with ethyl acetoacetate in the presence
Jain, A. C.,Mehta, A.,Arya, P.
p. 150 - 153
(2007/10/02)
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