{"product_id":"isoxazolidine-derivatives-synthesis-and-biological-activity-study-von-mohammed-al-ghorbani-usama-al-timari-taha-abu-bakr-fathl","title":"Isoxazolidine derivatives","description":"\u003cp\u003eBased 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.\u003c\/p\u003e\u003cdiv class=\"aw-variant-hidden-subtitle-div\" id=\"aw-variant-subtitle-9783330798342\"\u003e\u003ch3\u003eSynthesis and biological ¿activity study\u003c\/h3\u003e\u003c\/div\u003e","brand":"Libri","offers":[{"title":"Softcover - 9783330798342","offer_id":39426925789277,"sku":"9783330798342","price":49.9,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0940\/0622\/files\/e01c0d33-5740-4bd6-baa1-e0a483cbe87a.jpg?v=1774676025","url":"https:\/\/shop.autorenwelt.de\/products\/isoxazolidine-derivatives-synthesis-and-biological-activity-study-von-mohammed-al-ghorbani-usama-al-timari-taha-abu-bakr-fathl","provider":"Autorenwelt Shop","version":"1.0","type":"link"}