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Synthesis 2003(1): 0035-0040
DOI: 10.1055/s-2003-36246
DOI: 10.1055/s-2003-36246
PAPER
© Georg Thieme Verlag Stuttgart · New YorkSynthesis of Fluorinated Indolizines and 4H-Pyrrolo[1,2-a]benzimidazoles via 1,3-Dipolar Cycloaddition of Fluoroalkenes to N-Ylides
Further Information
Received
18 September 2002
Publication Date:
18 December 2002 (online)
Publication History
Publication Date:
18 December 2002 (online)

Abstract
In the presence of K2CO3 and Et3N, pyridinium, quinolinium, isoquinolinium and benzimidazolinium N-ylides, generated in situ from their halides, react with gaseous flouroalkenes [CF2=CFX (1), X = Cl (a), Br (b), CF3 (d)] in DMF under atmospheric pressure in normal glassware at 70 °C to give the corresponding fluorinated indolizines or H-pyrrolo[1,2-a]benzimidazoles via 1,3-dipolar [3+2] cycloaddition. Similar results are obtained with tetrafluoroethene in an autoclave.
Key words
1,3-dipolar addition - [3+2] cycloaddition - fluoroalkene - fluorinated indolizine - fluorinated H-pyrrolo[1,2-a]benzimidoazole
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