
Tetrahedron Letters p. 5715 - 5718 (1995)
Update date:2022-08-30
Topics:
Glick, HC
Likhotvorik, Igor R.
Jones, Maitland
Treatment of 7,7-dibromodibenzobicyclo<4.1.0>heptane with di-tert-butylcuprate or dibutylcuprate, followed by quenching with water, led to exo- and endo-7-monoalkyldibenzobicyclo<4.1.0>heptanes.Photolysis through either quartz or Pyrex gave the products of intramolecular reactions of the corresponding alkylcarbenes.The temperature dependence of the products formed from tert-butylcarbene was verified, and butylcarbene was trapped intermolecularly. - Keywords: carbenes, retrocycloadditions, insertion reactions.
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