Mohammed al ghorbani (4 resultados)

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Librería: Revaluation Books, Exeter, Reino UnidoRevaluation Books
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Paperback. Condición: Brand New. 124 pages. 8.66x5.91x0.28 inches. In Stock.

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Librería: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, AlemaniaBuchWeltWeit Ludwig Meier e.K.
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Taschenbuch. Condición: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Based on the regio and stereoselectivity of 1,3-dipolar cycloaddition reactions of nitrones to alkenes the book has focus on - regio and stereoselectivity synthesis of N-nucleosides by 1,3-dipolar cycloaddition of sugar-derived nitrones with N-arylmaleimides. - 1,3-Dipolar cycloaddition of N-ribosylnitrones and N-arylmalaimides affords anti-isoxazolidine. - A series of novel nitrones were prepared and isolated in a pure state, and they cycloadded to some allyl derivatives to give isoxazolidine derivatives and studied the stereoselectivity of their cycloaddition reactions. - Lewis acid (MgBr2.Et2O) was applied as a catalyst for 1,3-dipolar cycloaddition reactions and it highly effect the rate of cycloaddition reaction. - we studied also the biological activity of nitrone and isoxazolidine compounds. 124 pp. Englisch.…

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Librería: moluna, Greven, Alemaniamoluna
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Condición: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Al-Ghorbani Mohammed1. Dr. Mohammed Al-Ghorbani Assistant Professor Department of Chemistry University of Thamar, Yemen2. Prof. Dr. Usama Al-Timari Professor in Organic Chemistry College of Health and Medical Technolog.…

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Librería: buchversandmimpf2000, Emtmannsberg, BAYE, Alemaniabuchversandmimpf2000
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Envío por EUR 60,00Se envía de Alemania a Estados Unidos de AmericaCantidad disponible: 1 disponible
Taschenbuch. Condición: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Based on the regio and stereoselectivity of 1,3-dipolar cycloaddition reactions of nitrones to alkenes the book has focus on - regio and stereoselectivity synthesis of N-nucleosides by 1,3-dipolar cycloaddition of sugar-derived nitrones with N-arylmaleimides. - 1,3-Dipolar cycloaddition of N-ribosylnitrones and N-arylmalaimides affords anti-isoxazolidine. - A series of novel nitrones were prepared and isolated in a pure state, and they cycloadded to some allyl derivatives to give isoxazolidine derivatives and studied the stereoselectivity of their cycloaddition reactions. - Lewis acid (MgBr2.Et2O) was applied as a catalyst for 1,3-dipolar cycloaddition reactions and it highly effect the rate of cycloaddition reaction. - we studied also the biological activity of nitrone and isoxazolidine compounds.Books on Demand GmbH, Überseering 33, 22297 Hamburg 124 pp. Englisch.…