Abstract
The 1:1 reactive intermediates generated by the addition of alkyl isocyanides to dialkyl acetylenedicarboxylates were trapped by 4-hydroxy quinoline to yield highly functionalized 1-azabuta-1,3-dienes
Keywords: Acetylenic esters, alkyl isocyanides, 1-Azabuta-1,3-dienes, 4-Hydroxy quinoline, multi-component reaction, Isocyanides, hydroxyquinoline, alkyl, pyridinol
Letters in Organic Chemistry
Title: Reaction of Alkyl Isocyanides, Dialkyl Acetylenedicarboxylates with 4-Hydroxy Quinoline: Synthesis of 1-Azabuta-1,3-Dienes
Volume: 9 Issue: 2
Author(s): Bita Mohtat, Somayeh Rezazadeh, Mahnaz Matinfar, Vale Arabzadeh, Hoorieh Djahaniani and Zinatossadat Hossaini
Affiliation:
Keywords: Acetylenic esters, alkyl isocyanides, 1-Azabuta-1,3-dienes, 4-Hydroxy quinoline, multi-component reaction, Isocyanides, hydroxyquinoline, alkyl, pyridinol
Abstract: The 1:1 reactive intermediates generated by the addition of alkyl isocyanides to dialkyl acetylenedicarboxylates were trapped by 4-hydroxy quinoline to yield highly functionalized 1-azabuta-1,3-dienes
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Cite this article as:
Mohtat Bita, Rezazadeh Somayeh, Matinfar Mahnaz, Arabzadeh Vale, Djahaniani Hoorieh and Hossaini Zinatossadat, Reaction of Alkyl Isocyanides, Dialkyl Acetylenedicarboxylates with 4-Hydroxy Quinoline: Synthesis of 1-Azabuta-1,3-Dienes, Letters in Organic Chemistry 2012; 9 (2) . https://dx.doi.org/10.2174/157017812800221762
DOI https://dx.doi.org/10.2174/157017812800221762 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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