1047632-49-4Relevant articles and documents
Reaction products of methyl tricyclo[4.1.0.02,7]heptane-1- carboxylate and tricyclo[4.1.0.02,7]hept-1-yl phenyl sulfone with dinitrogen tetraoxide
Vasin,Kostryukov,Bolusheva,Razin
, p. 511 - 515 (2008)
The reaction of methyl tricyclo[4.1.0.02,7]hepatne-1-carboxylate with dinitrogen tetraoxide in diethyl ether at -10 to 0°C, followed by treatment of the reaction mixture with methanol, gave approximately equal amounts of methyl exo,syn-6,7-dinitro-and exo-6-hydroxy-syn-7-nitrobicyclo[3.1. 1]heptane-endo-6-carboxylates. Tricyclo[4.1.0.02,7]hept-1-yl phenyl sulfone reacted with dinitrogen tetraoxide under analogous conditions to produce a mixture of diastereoisomeric exo,syn-and endo,syn-6,7-dinitro-6- phenylsulfonylbicyclo-[3.1.1]heptanes and 6,6-dimethoxy-endo-7-nitrobicyclo[3.1. 1]heptane at a ratio of 4.5:2:1. Probable factors responsible for the different stereoselectivities in the addition of N2O4 at the central C1-C7 bond of the initial tricycloheptane compounds were discussed. The structural parameters of the dinitro ester and related dinitro sulfone were compared on the basis of the X-ray diffraction data.