Addition d'azlactones ylures d'azomethine potentiels aux esters acryliques et fumariques et au fumaronitrile : obtention de carbolactones.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. 1.3‐Dipolare Cycloadditionen, LV. Δ 1 ‐Pyrroline und 7‐Aza‐bicyclo[2.2.1]heptane aus Azlactonen und aktivierten Alkenen
2. Photochemical transformations of small ring heterocyclic compounds. XLVI. Scope of the photoinduced 1,3-dipolar addition reactions of arylazirines
3. Addition d'acides α amines a quelques composes ethyleniques actives, en milieu anhydride acetique. Obtention de pyrrolines-2 N acylees
4. O. Yebdri et F. Texier résultats non publiés.
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3. Intermolecular Dipolar Cycloaddition Reactions of 5H,7H-Thiazolo[3,4-c]oxazol-4-ium-1-olates;Tetrahedron;2000-05
4. Base-induced conversion of 5-aminothiazolium salts into substituted pyrroles and pyrrolines via 1,3-dipolar cycloadditions with electron-deficient alkynes and alkenes;Tetrahedron;1995-06
5. Intermolecular 1,3-dipolar cycloadditions of müchnones with acetylenic dipolarophiles: Sorting out the regioselectivity;Tetrahedron;1994-04
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