9786138829928 - preparation and reactions of racemic and optically active cyanohydrins: biological evaluation of some cyanohydrin derivatives as very potent anticancer von morsy mohamed, nesrin mahmoud; h. mahran, mohamed refat; a. yosef, hisham abdallah (8 Ergebnisse)
Preparation and Reactions of Racemic and Optically Active Cyanohydrins: Biological Evaluation of some Cyanohydrin derivatives as Very Potent anticancer
Morsy Mohamed, Nesrin Mahmoud; H. Mahran, Mohamed Refat; A. Yosef, Hisham Abdallah
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Taschenbuch. Zustand: 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.
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Taschenbuch. Zustand: 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 eno…rmous 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.
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Preparation and Reactions of Racemic and Optically Active Cyanohydrins
Nesrin Mahmoud Morsy Mohamed|Mohamed Refat H. Mahran|Hisham Abdallah A. Yosef
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Zustand: 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.
Preparation and Reactions of Racemic and Optically Active Cyanohydrins: Biological Evaluation of some Cyanohydrin derivatives as Very Potent anticancer
Morsy Mohamed, Nesrin Mahmoud; H. Mahran, Mohamed Refat; A. Yosef, Hisham Abdallah
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Preparation and Reactions of Racemic and Optically Active Cyanohydrins: Biological Evaluation of some Cyanohydrin derivatives as Very Potent anticancer
Morsy Mohamed, Nesrin Mahmoud; H. Mahran, Mohamed Refat; A. Yosef, Hisham Abdallah
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Taschenbuch. Zustand: 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 enormou…s 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.
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Taschenbuch. Zustand: 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.
