Department of Organic Chemistry, Karaj Branch, Islamic Azad university, Karaj, Iran
Abstract
The reactive intermediate generated by the addition of tert-butyl and 1,1,3,3-tetramethyl butyl isocyanide and cyclohexyl isocyanide to dialkyl acetylenedicarboxylate was trapped by 3-hydroxy pyridine to produce highly functionalized 4H-chromenes in fairly good yields
Mahpeyma, M., Mohtat, B. (2011). Reaction between 3-hydroxy pyridine alkyl isocyanides and dialkyl acetylenedicarboxylate: synthesis of 4H-chromenes. International Journal of Heterocyclic Chemistry, 1(3), 45-48.
MLA
Mahsa Mahpeyma; Bita Mohtat. "Reaction between 3-hydroxy pyridine alkyl isocyanides and dialkyl acetylenedicarboxylate: synthesis of 4H-chromenes". International Journal of Heterocyclic Chemistry, 1, 3, 2011, 45-48.
HARVARD
Mahpeyma, M., Mohtat, B. (2011). 'Reaction between 3-hydroxy pyridine alkyl isocyanides and dialkyl acetylenedicarboxylate: synthesis of 4H-chromenes', International Journal of Heterocyclic Chemistry, 1(3), pp. 45-48.
VANCOUVER
Mahpeyma, M., Mohtat, B. Reaction between 3-hydroxy pyridine alkyl isocyanides and dialkyl acetylenedicarboxylate: synthesis of 4H-chromenes. International Journal of Heterocyclic Chemistry, 2011; 1(3): 45-48.
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