1,3-DIPOLAR CYCLOADDITION REACTIONS OF SOME 1-ARYL-PYRIDINIUM-3-OLATES

Date

1993-07-01

Author

CELEBI, N
CETINER, O
GULEC, A
Türker, Burhan Lemi

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In this study, the reactivities of 1-(2,4-dinitrophenyl)-, 1-(4,6-dimethylpyrimidin-2-yl)-, and 1-(5-nitro-2-pyridyl)-pyridinium-3-olates were tested upon various inductively and mesomerically electron rich dipolarophiles. N-substituted pyridinium-3-olates react across the 2,6-positions with 2pi-dipolarophiles whereas 4pi-dipolarophiles added across both 2,6 and 2,4 positions of the betaines.

Subject Keywords

General Chemistry

URI

https://hdl.handle.net/11511/62919

Journal

BULLETIN DES SOCIETES CHIMIQUES BELGES

DOI

https://doi.org/10.1002/bscb.19931020706

Collections

Department of Chemistry, Article

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Citation Formats

N. CELEBI, O. CETINER, A. GULEC, and B. L. Türker, “1,3-DIPOLAR CYCLOADDITION REACTIONS OF SOME 1-ARYL-PYRIDINIUM-3-OLATES,” BULLETIN DES SOCIETES CHIMIQUES BELGES, pp. 467–477, 1993, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/62919.