A Facile and Efficient Reaction of Aromatic Aldehydes with the Isocyanide- Dialkylacetylenedicarboxylate Zwitter Ions: Formation of 2-Amino-5-aryl Furan Derivatives
Corresponding Author(s) : Sakineh Asghari
s.asghari@umz.ac.ir
Asian Journal of Chemistry,
Vol. 22 No. 5 (2010): Vol 22 Issue 5
Abstract
The 1:1 intermediate generated by the addition of t-butyl isocyanide to dialkyl acetylene dicarboxylate is trapped by various aromatic aldehydes to yield 2-amino-5-aryl furan derivatives.
Keywords
tert-Butyl isocyanide
Benzaldehyde
Furfural
Biphenyl carbaldehyde
2-Amino-5aryl furan
Asghari, S., & Qandalee, M. (2010). A Facile and Efficient Reaction of Aromatic Aldehydes with the Isocyanide- Dialkylacetylenedicarboxylate Zwitter Ions: Formation of 2-Amino-5-aryl Furan Derivatives. Asian Journal of Chemistry, 22(5), 3435–3438. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/11566
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