The reactivity of 1,4-dihydronicotinamides towards reduction of 1,1′,1″-trifluoro-acetophenone : influence of methyl substitution on the pyridine ring.

Bossaerts, J.; Dommisse, Roger; Alderweireldt, F. C.

doi:10.1016/s0040-4039(01)80219-7

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The reactivity of 1,4-dihydronicotinamides towards reduction of 1,1′,1″-trifluoro-acetophenone : influence of methyl substitution on the pyridine ring.

Cited by 3 publications

References 8 publications

ChemInform Abstract: THE REACTIVITY OF 1,4‐DIHYDRONICOTINAMIDES TOWARDS REDUCTION OF 1,1′,1“‐TRIFLUOROACETOPHENONE: INFLUENCE OF METHYL SUBSTITUTION ON THE PYRIDINE RING

ChemInform Abstract: THE REACTIVITY OF 1,4‐DIHYDRONICOTINAMIDES TOWARDS REDUCTION OF 1,1′,1“‐TRIFLUOROACETOPHENONE: INFLUENCE OF METHYL SUBSTITUTION ON THE PYRIDINE RING

References

NADH mimics for the stereoselective reduction of benzoylformates to the corresponding mandelates.

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