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Titlebook: Enzymes as Catalysts in Organic Synthesis; M. P. Schneider Book 1986 D. Reidel Publishing Company, Dordrecht, Holland 1986 carbon.natural

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楼主: 债权人
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https://doi.org/10.1007/978-3-319-60943-0nnatural cyclopentanoids using the meso-concept and an efficient enzyme catalysed asymmetric transformation is described. . serves as a common intermediate for the asymmetric total synthesis of the macrolides brefeldin A . and 7-epi-brefeldin A .as well as the new prostaglandin building block .
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https://doi.org/10.1007/978-3-658-30762-2 strategy developed here is based on symmetri-zatlon-asymmetrization concept. Thus, retrosynthesls was carried out to generate, from target molecules, simplified symmetric diesters (symmetrization), and then the symmetric diesters were subjected to asymmetric hydrolysis with pig liver esterase to cr
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Agency: Its Terms and Relations,etol products of high enantiomeric excess. The scope and versatility of this method for a variety of substrates was examined and the integration of selected microbial products in synthetic strategies to various natural products including the trichothecene mycotoxins was illustrated. Yeast reduction
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Choice-Relevant Diversity Revealed,rpose, glycosyl-lithium reagents have been prepared from thio-phenyl glycosides, anomeric sulfones, or glycosylstannanes. They react in a stereocontrolled manner with aldehydes to provide, after opening of the tetrahydropyran ring, the expected higher sugars.
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Jesús H. Aguilar,Andrei Buckareffnds formed serve as homoenolate reagents and add to aldehydes and ketones with high γ-regioselectivity to yield enol carb-amates of 4-oxy-alkanals or -alkanones. After exchange of the cation by titanium or aluminium reagents, the addition proceeds with high. or . diastereoselectivity. Altogether, th
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Artwork Authorship as a Sign-in-Action-specific carbon-carbon bond formation catalyzed by aldolases is one of the most efficient and practical route to common and uncommon sugar derivatives. Detailed studies on the synthetic application of FDP aldolase-catalyzed condensation indicate that enzymatic aldol reactions seem to have genuine v
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https://doi.org/10.1007/978-3-531-93092-3thylsulfatase, N,N-dimethylformamidase (DMFase), esterases, methanol dehydrogenase etc. The properties and possible applications of these microbes and enzymes are discussed. Mutant strains of . (rifamycin producer) were successfully applied for the microbial production of D(−)-ribulose and shikimic
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https://doi.org/10.1007/978-3-662-66439-1ed as starting materials in syntheses of stereospecifically labelled samples of serine, glutamic acid, 2-aminoethanol, β-alanine and 2-fluoropropanoic acid. The latter compounds have been used to study the stereochemistry of some enzyme catalysed reactions. The enzymes glutamate pyruvate transaminas
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