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Reduction by a model of NAD(P)H. Contribution of metal ion to asymmetric reduction of trifluoroacetophenone

โœ 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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โœฆ 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


๐Ÿ“œ SIMILAR VOLUMES


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โœ Yutaka Ohnishi; Miyoko Kitami ๐Ÿ“‚ Article ๐Ÿ“… 1978 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 158 KB

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