Preparation and Reactions of Racemic and Optically Active Cyanohydrins: Biological Evaluation of some Cyanohydrin derivatives as Very Potent anticancer - Brossura
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Chiral (R)-, (S)-cyanohydrins are widespread in nature in the form of the respective glycosides and serve roughly 3000 plants and many insects as antifeedants. For the preparative organic chemist, this class of compounds offers an enormous synthetic potential for making other chiral compounds accessible. In a few instances, the pharmacological principle of a drug also incorporates a chiral cyanohydrin as constitutive structural element. The development of simple synthetic procedures for cyanohydrins, which also entail a high degree of stereoselectivity, therefore has prime importance. In this respect, chiral cyanohydrins may serve as stereochemically pure starting materials Stereoselective follow–up of (R)–and (S)–cyanohydrins lead to other important classes of compounds with stereogenic centeres. Thus, starting from (R)–cyanohydrins, (R)–2–hydroxyaldehydes, (R)–2–hydroxyketones, (1R)–2–aminoalcohols and (1R, 2S)–2–aminoalcohols are easily obtained in high optical and chemical yields by appropriate transformations of the cyano–group.cyanohydrins can also produce optically active tertiary α–hydroxycarboxylic acid
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Preparation and Reactions of Racemic and Optically Active Cyanohydrins
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Scholars' Press Mai 2019, 2019
ISBN 10: 6138829921
ISBN 13: 9786138829928
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Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Chiral (R)-, (S)-cyanohydrins are widespread in nature in the form of the respective glycosides and serve roughly 3000 plants and many insects as antifeedants. For the preparative organic chemist, this class of compounds offers an enormous synthetic potential for making other chiral compounds accessible. In a few instances, the pharmacological principle of a drug also incorporates a chiral cyanohydrin as constitutive structural element. The development of simple synthetic procedures for cyanohydrins, which also entail a high degree of stereoselectivity, therefore has prime importance. In this respect, chiral cyanohydrins may serve as stereochemically pure starting materials Stereoselective follow-up of (R)-and (S)-cyanohydrins lead to other important classes of compounds with stereogenic centeres. Thus, starting from (R)-cyanohydrins, (R)-2-hydroxyaldehydes, (R)-2-hydroxyketones, (1R)-2-aminoalcohols and (1R, 2S)-2-aminoalcohols are easily obtained in high optical and chemical yields by appropriate transformations of the cyano-group.cyanohydrins can also produce optically active tertiary -hydroxycarboxylic acid 188 pp. Englisch. Codice articolo 9786138829928
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Preparation and Reactions of Racemic and Optically Active Cyanohydrins
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Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Morsy Mohamed Nesrin MahmoudAss. Prof. Dr. Nesrin Mahmoud Morsy is an assistant professor in Organometallic and Organometalloid Chemistry Department. Prof.Dr. Mohamed Refat H. Mahran and prof. Dr. Hisham Abdallah A. Yosef. Both of t. Codice articolo 290523569
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Preparation and Reactions of Racemic and Optically Active Cyanohydrins: Biological Evaluation of some Cyanohydrin derivatives as Very Potent anticancer
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Preparation and Reactions of Racemic and Optically Active Cyanohydrins: Biological Evaluation of some Cyanohydrin derivatives as Very Potent anticancer
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Preparation and Reactions of Racemic and Optically Active Cyanohydrins | Biological Evaluation of some Cyanohydrin derivatives as Very Potent anticancer
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Taschenbuch. Condizione: Neu. Preparation and Reactions of Racemic and Optically Active Cyanohydrins | Biological Evaluation of some Cyanohydrin derivatives as Very Potent anticancer | Nesrin Mahmoud Morsy Mohamed (u. a.) | Taschenbuch | 188 S. | Englisch | 2019 | Scholars' Press | EAN 9786138829928 | Verantwortliche Person für die EU: BoD - Books on Demand, In de Tarpen 42, 22848 Norderstedt, info[at]bod[dot]de | Anbieter: preigu. Codice articolo 116773943
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Preparation and Reactions of Racemic and Optically Active Cyanohydrins: Biological Evaluation of some Cyanohydrin derivatives as Very Potent anticancer
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Preparation and Reactions of Racemic and Optically Active Cyanohydrins
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Scholars' Press Mai 2019, 2019
ISBN 10: 6138829921
ISBN 13: 9786138829928
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Taschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Chiral (R)-, (S)-cyanohydrins are widespread in nature in the form of the respective glycosides and serve roughly 3000 plants and many insects as antifeedants. For the preparative organic chemist, this class of compounds offers an enormous synthetic potential for making other chiral compounds accessible. In a few instances, the pharmacological principle of a drug also incorporates a chiral cyanohydrin as constitutive structural element. The development of simple synthetic procedures for cyanohydrins, which also entail a high degree of stereoselectivity, therefore has prime importance. In this respect, chiral cyanohydrins may serve as stereochemically pure starting materials Stereoselective follow-up of (R)-and (S)-cyanohydrins lead to other important classes of compounds with stereogenic centeres. Thus, starting from (R)-cyanohydrins, (R)-2-hydroxyaldehydes, (R)-2-hydroxyketones, (1R)-2-aminoalcohols and (1R, 2S)-2-aminoalcohols are easily obtained in high optical and chemical yields by appropriate transformations of the cyano-group.cyanohydrins can also produce optically active tertiary ¿-hydroxycarboxylic acidVDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 188 pp. Englisch. Codice articolo 9786138829928
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Preparation and Reactions of Racemic and Optically Active Cyanohydrins : Biological Evaluation of some Cyanohydrin derivatives as Very Potent anticancer
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Taschenbuch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Chiral (R)-, (S)-cyanohydrins are widespread in nature in the form of the respective glycosides and serve roughly 3000 plants and many insects as antifeedants. For the preparative organic chemist, this class of compounds offers an enormous synthetic potential for making other chiral compounds accessible. In a few instances, the pharmacological principle of a drug also incorporates a chiral cyanohydrin as constitutive structural element. The development of simple synthetic procedures for cyanohydrins, which also entail a high degree of stereoselectivity, therefore has prime importance. In this respect, chiral cyanohydrins may serve as stereochemically pure starting materials Stereoselective follow-up of (R)-and (S)-cyanohydrins lead to other important classes of compounds with stereogenic centeres. Thus, starting from (R)-cyanohydrins, (R)-2-hydroxyaldehydes, (R)-2-hydroxyketones, (1R)-2-aminoalcohols and (1R, 2S)-2-aminoalcohols are easily obtained in high optical and chemical yields by appropriate transformations of the cyano-group.cyanohydrins can also produce optically active tertiary -hydroxycarboxylic acid. Codice articolo 9786138829928
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