Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. The appropriate choice can avoid electrode passivation, which strongly inhibit the efficient activation of substrates. 125995-03-1, Name is Atorvastatin lactone, molecular formula is C33H33FN2O4. In a Article,once mentioned of 125995-03-1, Formula: C33H33FN2O4
A series of trans-tetrahydro-4-hydroxy-6-<2-(2-(2,3,4,5-substituted-1H-pyrrol-1-yl)ethyl>-2H-pyran-2 ones and their dihydroxy acids were prepared and tested for their ability to inhibit the enzyme HMG-CoA reductase in vitro.Inhibitory potency was found to increase subtantially when substituents were introduced into positions three and four of the pyrrole ring.A systematic exploration of structure-activity relationships at these two positions led to the identification of a compound ((+)-33, (+)-(4R)-trans-2-(4-fluorophenyl)-5-(1-methylethyl)-N,3-diphenyl-1-<(tetrahydro-4-hydroxy-6-oxo-2H-pyran-2-yl)ethyl> -1H-pyrrole-4-carboxamide) with five times the inhibitory potency of the fungal metabolite compactin.
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Reference:
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics