Reduction by a model of NAD(P)H. Contribution of metal ion to asymmetric reduction of trifluoroacetophenone
โ Scribed by Yutaka Ohnishi; Takashi Numakunai; Atsuyoshi Ohno
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- French
- Weight
- 124 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
In spite of tremendous works on mimetic reactions of NAD(P)H-dependent dehydrogenases, 1 stereochemical problem has not been paid much attention.
Recently, we reported that optically active 1,4-dihydronicotinamide derivatives, in which the chiral center is separated from the reaction center by five atoms, results in asymmetric reduction of a-keto esters by the aid of magnesium or zinc perchlorate.
2 We wish now to present the stereochemical results from the reaction of a,a,a-trifluoroacetophenone
๐ SIMILAR VOLUMES
With respect to enzymatic reductions of carbonyl compounds by reduced pyridine nucleotides,NAD(P)H,wedescribedpreviouslychemicalreduction, assisted by a divalent metal ion such as Mg++ or Zn ++,of a-keto esters with 1-benzyl-1,4dihydronicotinamide(BNAH) as a model of NAD(P)H'! This mimicry has beene