cheminform abstract: 1,3-dipolar cycloadditions. part 107. cycloadditions of isoquinolinium...

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1998 fused pyridine derivatives fused pyridine derivatives R 0450 49 - 182 1,3-Dipolar Cycloadditions. Part 107. Cycloadditions of Isoquino- linium N-Arylimides to Enamines. — The cycloaddition products described are in a cycloaddition-cycloreversion equilibrium. Thus, yields are not quantitative as in the case of the reaction with electrophilic C=C bonds. — (HUISGEN, R.; DURST, T.; TEMME, R.; J. Heterocycl. Chem. 35 (1998) 3, 637-642; Inst. Org. Chem., Ludwig-Maximilians-Univ., D-80333 Muenchen, Germany; EN) 1

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Page 1: ChemInform Abstract: 1,3-Dipolar Cycloadditions. Part 107. Cycloadditions of Isoquinolinium N-Arylimides to Enamines

1998 fused pyridine derivatives

fused pyridine derivativesR 0450

49 - 1821,3-Dipolar Cycloadditions. Part 107. Cycloadditions of Isoquino-linium N-Arylimides to Enamines. — The cycloaddition productsdescribed are in a cycloaddition-cycloreversion equilibrium. Thus, yields arenot quantitative as in the case of the reaction with electrophilic C=C bonds.— (HUISGEN, R.; DURST, T.; TEMME, R.; J. Heterocycl. Chem. 35 (1998)3, 637-642; Inst. Org. Chem., Ludwig-Maximilians-Univ., D-80333 Muenchen,Germany; EN)

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Page 2: ChemInform Abstract: 1,3-Dipolar Cycloadditions. Part 107. Cycloadditions of Isoquinolinium N-Arylimides to Enamines

1998 fused pyridine derivatives

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