Article ID Journal Published Year Pages File Type
1314320 Journal of Fluorine Chemistry 2012 5 Pages PDF
Abstract

The three-component reactions (TCRs) involving quinoline or isoquinoline, dialkyl acetylenedicarboxylate and β-trifluoroacetyl vinyl ethyl ether were investigated. The reaction proceeded smoothly under ambient temperature in DMSO to give the 4-trifluoroacetyl substituted benzo[c]quinolizine derivatives in moderate yields. However, under the same reaction condition, isoquinoline afforded the 2-trifluoromethyl substituted 1-oxa-(11H)-benzo[a]dihydroquinolizine or 4-trifluoroacetyl substituted benzo[a]dihydroquinolizine products. The possible reaction pathways were proposed.

Graphical abstractThe three-component reactions (TCRs) involving quinoline or isoquinoline, dialkyl acetylenedicarboxylate and β-trifluoroacetyl vinyl ethyl ether were investigated. The reaction proceeded smoothly under ambient temperature in DMSO to give the 4-trifluoroacetyl substituted benzo[c]quinolizine derivatives in moderate yields. However, under the same reaction condition, isoquinoline afforded the 2-trifluoromethyl substituted 1-oxa-(11H)-benzo[a]dihydroquinolizine or 4-trifluoroacetyl substituted benzo[a]dihydroquinolizine products. The possible reaction pathways were proposed.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► A three-component reaction was investigated. ► The reaction proceeded smoothly under ambient temperature in DMSO. ► Quinolines afforded the CF3CO-substituted benzoquinolizines. ► But isoquinolines and DMAD gave the CF3-substituted 1-oxa-benzodihydroquinolizines. ► The possible reaction pathways were proposed.

Related Topics
Physical Sciences and Engineering Chemistry Inorganic Chemistry
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