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Titlebook: Enzymatic Reactions in Organic Media; A. M. P. Koskinen (Professor of Organic Chemistry) Book 1996 Chapman & Hall 1996 Resol.organic chemi

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書目名稱Enzymatic Reactions in Organic Media
編輯A. M. P. Koskinen (Professor of Organic Chemistry)
視頻videohttp://file.papertrans.cn/314/313041/313041.mp4
圖書封面Titlebook: Enzymatic Reactions in Organic Media;  A. M. P. Koskinen (Professor of Organic Chemistry) Book 1996 Chapman & Hall 1996 Resol.organic chemi
描述The outlook of organic synthesis has changed many times during its tractable history. The initial focus on the synthesis of substances typical of living matter, exemplified by the first examples of organic chemistry through the synthesis of urea from inorganic substances by Liebig, was accepted as the birth of organic chemistry, and thus also of organic synthesis. Although the early developments in organic synthesis closely followed the pursuit of molecules typical in nature, towards the end of the 19th century, societal pressures placed higher demands on chemical methods appropriate for the emerging age of industrialization. This led to vast amounts of information being generated through the discovery of synthetic reactions, spectroscopic techniques and reaction mechanisms. The basic organic functional group transformations were discovered and improved during the early part of this century. Reaction mechanisms were elucidated at a growing pace, and extremely powerful spectroscopic tools, such as infrared, nuclear magnetic resonance and mass spectrometry were introduced as everyday tools for a practising organic chemist. By the 1950s, many practitioners were ready to agree that alm
出版日期Book 1996
關鍵詞Resol; organic chemistry; polymer; polymerization; synthesis
版次1
doihttps://doi.org/10.1007/978-94-011-0611-5
isbn_softcover978-94-010-4269-7
isbn_ebook978-94-011-0611-5
copyrightChapman & Hall 1996
The information of publication is updating

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Fundamentals of non-aqueous enzymology,phobic substrates, ease of product and enzyme recovery, and reduced risk of microbial contamination of reactors. In order to take full advantage of these perceived benefits of non-aqueous enzymology, we must first understand the fundamental interaction between a solvent and an enzyme. The structural
地板
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https://doi.org/10.1007/b115016phobic substrates, ease of product and enzyme recovery, and reduced risk of microbial contamination of reactors. In order to take full advantage of these perceived benefits of non-aqueous enzymology, we must first understand the fundamental interaction between a solvent and an enzyme. The structural
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https://doi.org/10.1007/978-1-4615-9044-6condensation, where side chain protection-deprotection and racemization through carboxyl terminus activation by chemical methods are serious problems (4). One of the most successful examples of protease-catalyzed peptide segment condensation can be found in a semi-synthesis of insulin (5).
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Regioselectivity of hydrolases in organic media, These findings further enlighten the versatility of lipases and proteases, enzymes able to interact with substrates that are structurally unrelated to their natural targets, triacylglicerides and proteins respectively.
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Peptide synthesis,condensation, where side chain protection-deprotection and racemization through carboxyl terminus activation by chemical methods are serious problems (4). One of the most successful examples of protease-catalyzed peptide segment condensation can be found in a semi-synthesis of insulin (5).
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Modes of using enzymes in organic media,drophilic substances present in the aqueous phase while hydrophobic substrates and products mainly partition to the organic phase (Figure 2.1). In order for the bioconversion to occur, the substrates must be transferred to the enzyme in the aqueous phase. After the reaction, hydrophobic products are transferred back to the organic phase.
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