Comparative inhibition of tetrameric carbonyl reductase activity in pig heart cytosol by alkyl 4-pyridyl ketones
Context and objective: The present study is to elucidate the comparative inhibition of tetrameric carbonyl reductase (TCBR) activity by alkyl 4-pyridyl ketones, and to characterize its substrate-binding domain. Materials and methods: The inhibitory effect
The anion of 4-dimethoxymethylpyridine. A convenient synthesis of some 4-pyridyl ketones
n-Butyllithium at -78°C abstracts the methine proton from 4-dimethoxymethylpyridine. The anion reacts efficiently with electrophiles. Simple ketal products can be readily hydrolysed to 4-pyridyl ketones.
Sheldrake
p. 1967 - 1971
(2007/10/02)
More Articles about upstream products of 32941-30-3