Helvetica Chimica Acta p. 1497 - 1503 (1990)
Update date:2022-08-16
Topics:
Neidlein, Richard
Kohl, Matthias
1,1-Difluoro-1H-cyclopropabenzene (1) can be deprotonated with strong bases at C(2).The resulting 1,1-difluoro-2-lithio-1H-cyclopropabenzene (2) reacts with electrophiles to form C(2)-substituted derivatives of 1.The Diels-Alder reactions with electron-poor dienes, characteristic for 1H-cyclopropabenzene, do not occur with the 1,1-difluoro analogue of 1.
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