1, 2-Bridged cyclopropenes

KB Wiberg, DR Artis, G Bonneville

Index: Wiberg, Kenneth B.; Artis, Dean R.; Bonneville Journal of the American Chemical Society, 1991 , vol. 113, # 21 p. 7969 - 7979

Full Text: HTML

Citation Number: 40

Abstract

Abstract: The dehalogenations of 1, 5-dihalobicyclo [3.1. O] hexanes and 1, 6-dihalobicyclo [4.1. O] heptanes have been studied in solution and in the gas phase. The solution reactions led to the formation of bicycl0 [3. lO] hex-l (5)-ene and bicyclo-[4. I. O] hept-l (6)-ene, respectively, but this was followed by rapid ene reactions forming dimers, which then coupled to form tetramers. The cyclopropenes could be trapped as Diels-Alder adducts. In ...

Related Articles:

Bicyclo [3.1. 0] hex-(1, 5)-ene and bicyclo [4.1. 0] hept-(1, 6)-ene

[Kenneth, B. Wiberg; Bonneville, George Tetrahedron Letters, 1982 , vol. 23, # 51 p. 5385 - 5388]

More Articles...