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Titlebook: Microbial Reagents in Organic Synthesis; Stefano Servi Book 1992 Springer Science+Business Media Dordrecht 1992 Amino acid.Monosaccharid.O

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發(fā)表于 2025-3-21 19:50:06 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱Microbial Reagents in Organic Synthesis
編輯Stefano Servi
視頻videohttp://file.papertrans.cn/634/633026/633026.mp4
叢書(shū)名稱Nato Science Series C:
圖書(shū)封面Titlebook: Microbial Reagents in Organic Synthesis;  Stefano Servi Book 1992 Springer Science+Business Media Dordrecht 1992 Amino acid.Monosaccharid.O
出版日期Book 1992
關(guān)鍵詞Amino acid; Monosaccharid; Oxidation; enzymes; natural product
版次1
doihttps://doi.org/10.1007/978-94-011-2444-7
isbn_softcover978-94-010-5078-4
isbn_ebook978-94-011-2444-7Series ISSN 1389-2185
issn_series 1389-2185
copyrightSpringer Science+Business Media Dordrecht 1992
The information of publication is updating

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A Building Block Strategy for Asymmetric Synthesis: The DHAP-Aldolasestional chiral centers, in subsequent enzymatic conversions of aldolase generated products, or in the assembly of aldolase-based complex multi-enzyme cascade reactions that exploit renewable resources as precursors for simple one-pot syntheses.
地板
發(fā)表于 2025-3-22 05:06:22 | 只看該作者
A Direct Route from Hydantoins to D-Amino Acids Employing a Resting Cell Biocatalyst With D-Hydantoition rate constants of different hydantoins to challenge the widely held assumption of spontaneous racemization of hydantoins. We then explore the optimization of process parameters for high yield and selectivity. Finally, the broad substrate specificity and very good enantioselectivity of the biocatalyst are discussed.
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Transferase Catalyzed Synthesis: Applications in Series of Aminoacids and Monosaccharidestolase led to analogs of ketoses by transfer of an hydroxyacetyl group on an aldehyde. Various analogs of L-erythrulose and D-xylulose have been obtained. Transketolase also led to aldoses, such as D-threose and L-glucose by transfer of a formyl group on an aldehyde.
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發(fā)表于 2025-3-22 23:46:51 | 只看該作者
Enzymatic Aminolysis, Hydrazinolysis and Oximolysis Reactions are hydrazines with electronwithdrawing groups with which it is possible to obtain Naminosuccinimide derivatives from dimethyl succinate. The lipase catalyzed oximolysis reaction is a very efficient method to prepare oxime esters and oxime .-butylcarbonates from oximes and vinyl esters and .-butylpyrocarbonates respectively.
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(R)- and (S)-Cyanohydrins - Their Enzymatic Synthesis and Their Reactionsobtained. These nitriles react with various nucleophiles by complete inversion of configuration to form various α-substituted carboxylic acid derivatives, α-azido nitriles, α-amino nitriles, α-amino acids, etc.
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