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• W1463463130 endingPage "308" @default.
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• W1463463130 abstract "The biochemical field and its enormous potential are generating increasing interest, particularly among the chemists engaged in asymmetric syntheses. Thousands of microbiological and enzymic transformation of chemical significance are documented in excellent monograph. Enzymes are usually very selective with respect to the reaction type and substrate structure. Biochemical methods of effecting the chemical transformations are expensive. Some enzymes require nonprotein coenzymes for catalytic activity. Some coenzymes present little or no problem in this regard, because they are automatically reformed under the normal aqueous reaction conditions or in the presence of oxygen. These include biotin, pyridoxal phosphate (PLP), thiamine pyrophosphate, flavin mononucleotide (FM), and flavin adenine dinucleotide (FAD). A good knowledge of the principles and techniques of both organic chemistry and biochemistry is highly desirable, but an extensive background in microbiology is not necessary for experimental procedures. Carrying out fermentations and working with immobilized enzymes and microorganisms require a chemist to develop some new skills that are easily acquired. Controlled and stereospecific hydroxylation at inactivated carbon is easily achieved using fungi. The chance of finding an appropriate microorganism for a given hydroxylation is improved if a suitable literature analogy is found. Immobilization does not destroy hydroxylase activity. Hydroxylations of aromatic substrates follow the rules of electrophilic substitution. Chymotrypsin is the best documented hydrolase." @default.
• W1463463130 created "2016-06-24" @default.
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• W1463463130 date "1977-01-01" @default.
• W1463463130 modified "2023-10-14" @default.
• W1463463130 title "Chapter 30. Biochemical Procedures in Organic Synthesis" @default.
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• W1463463130 doi "https://doi.org/10.1016/s0065-7743(08)61569-9" @default.
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