TY - JOUR
T1 - Formation of a novel cyclopenta[b]pyran derivative in the dehydrobromination of 1,10-dibromobicyclo[8.1.0]undecane-3,8-dione
AU - Byrne, Lindsay
AU - Payne, A.D.
AU - Roemkens, C.H.
AU - Wege, Dieter
PY - 1999
Y1 - 1999
N2 - Treatment of 1,10-dibromobicyclo[8.1.0]undecane-3,8-dione (3) with triethylamine in dichloromethane results in the formation of a deep red compound formulated as 1,4,5,6,7,10,11,12,13,15b-decahydroazuleno[1',2'-e]cyclopropa[3,4]cyclodeca[1,2-b]pyran-3,14-dione (13) on the basis of its spectral properties.
AB - Treatment of 1,10-dibromobicyclo[8.1.0]undecane-3,8-dione (3) with triethylamine in dichloromethane results in the formation of a deep red compound formulated as 1,4,5,6,7,10,11,12,13,15b-decahydroazuleno[1',2'-e]cyclopropa[3,4]cyclodeca[1,2-b]pyran-3,14-dione (13) on the basis of its spectral properties.
U2 - 10.1071/CH98177
DO - 10.1071/CH98177
M3 - Article
SN - 0004-9425
VL - 52
SP - 395
EP - 401
JO - Australian Journal of Chemistry
JF - Australian Journal of Chemistry
IS - N/A
ER -