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Titlebook: Mechanistic Models of Asymmetric Reductions; Atsuyoshi Ohno,Satoshi Ushida Book 1986 Springer-Verlag Berlin Heidelberg 1986 Coenzym.amino

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发表于 2025-3-21 19:14:52 | 显示全部楼层 |阅读模式
书目名称Mechanistic Models of Asymmetric Reductions
编辑Atsuyoshi Ohno,Satoshi Ushida
视频video
丛书名称Lecture Notes in Bio-Organic Chemistry
图书封面Titlebook: Mechanistic Models of Asymmetric Reductions;  Atsuyoshi Ohno,Satoshi Ushida Book 1986 Springer-Verlag Berlin Heidelberg 1986 Coenzym.amino
描述Bio-organic Chemistry has corne of age - the sign of this is the start of a new series of Lecture Notes that are the product and substrate of spreading this line of modern knowledge among graduate students and research workers in such fields as mechanistic biochemistry, bio­ mimetic organic chemistry, biotechnological application of enzymology, to name only a few examples of how many frontiers are opened and borders lifted - just at. the time when the demand for a‘‘‘Synthetic Biology" and "Molecular Biotechnology" is increasing - fields that have been neglected for (too) long a time by "classical" chemists in curricula and imagination. We hope that through this first volume, which pOints in the several directions mentioned above, the profile of the undertaking will become clear and that it will find resonance among the scientific community interested in the thoughtful application of chemical and physical con­ cepts to biochemical and molecular-biological problems.
出版日期Book 1986
关键词Coenzym; amino acid; biochemistry; biology; chemistry; chirality; enzyme; enzymes; organic chemistry; synthes
版次1
doihttps://doi.org/10.1007/978-3-642-48868-9
isbn_softcover978-3-540-16440-1
isbn_ebook978-3-642-48868-9
copyrightSpringer-Verlag Berlin Heidelberg 1986
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Polar Effect Exerted by Other Asymmetric Reactions,rabatsos et al. 1967), Felkin model (Chérest et al. 1968, Chérest and Felkin 1968), and other similar models are stereo-models for transition states that predict the stereochemistry of the reaction from the viewpoint of a steric effect.
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NAD(P)H as a Coenzyme,-glycosidic bond* acts as a shuttle redox reagent by interconverting between 1,4-dihydropyridine and pyridinium cation structures. The remaining part of the coenzyme mainly acts as the binding site for the apoenzyme.
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Enzymatic Reductions,1970a,b). The replacement of only one of the six amino acids by another one results in the appearance of steroid activity (Eklund et al. 1976). It seems that the steroid activity is an intrinsic property of the enzyme rather than the activity toward ethanol because the latter is not a normal bodily constituent (Damgaard 1981).
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f spreading this line of modern knowledge among graduate students and research workers in such fields as mechanistic biochemistry, bio­ mimetic organic chemistry, biotechnological application of enzymology, to name only a few examples of how many frontiers are opened and borders lifted - just at. th
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Book 1986g this line of modern knowledge among graduate students and research workers in such fields as mechanistic biochemistry, bio­ mimetic organic chemistry, biotechnological application of enzymology, to name only a few examples of how many frontiers are opened and borders lifted - just at. the time whe
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Introduction,ety of reducing agents with the hope of extending their reducing power and of improving the selectivity to be utilized for modern organic synthesis. However, much better reductions had been taking place in living organisms for a long time before people developed organic chemistry. These reactions ar
发表于 2025-3-23 08:41:46 | 显示全部楼层
NAD(P)H as a Coenzyme, oxidized and reduced forms are depicted above. Within the coenzyme molecule, the nicotinamide moiety which is linked with a ribose moiety through a β-glycosidic bond* acts as a shuttle redox reagent by interconverting between 1,4-dihydropyridine and pyridinium cation structures. The remaining part
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