A queer product of the Beirut reaction with dimedone-AM1 analysis

Date

2002-09-27

Author

Türker, Burhan Lemi
Dura, E

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Dimedone reacted with benzofuraxane in the presence of Et3N. The expected products were quinoxaline derivatives but an unexpected compound was obtained in low yield. The structural identification of the product was done spectrally and a mechanism for its formation was proposed by the aid of AM l type semiempirical calculations.

Subject Keywords

AM1 calculations, Dimedone, Beirut reaction, Benzofurazan oxide

URI

https://hdl.handle.net/11511/62447

Journal

JOURNAL OF MOLECULAR STRUCTURE-THEOCHEM

DOI

https://doi.org/10.1016/s0166-1280(02)00311-1

Collections

Department of Chemistry, Article

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Citation Formats

B. L. Türker and E. Dura, “A queer product of the Beirut reaction with dimedone-AM1 analysis,” JOURNAL OF MOLECULAR STRUCTURE-THEOCHEM, pp. 143–147, 2002, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/62447.