1005-51-2Relevant articles and documents
SITE SELECTIVITY IN THE REACTIONS OF 1,3-DIPOLES AND DIENES WITH TETRACYCLO2,10.03,6>DODECA-4,8,11-TRIENE
Burdisso, M.,Gamba, A.,Gandolfi, R.,Pevarello, P.
, p. 4355 - 4360 (2007/10/02)
1,3-Dipoles and dienes reacted smoothly with excess tetracyclo2,10.03,6>dodeca-4,8,11-triene (1) to give good yields of monoadducts in a highly selective reaction.The attack by 1,3-dipoles and dienes to 1 occurred only at the
N-Phenyltriazolinedione Adducts of Bicyclodecatetraene and Tricyclo2,8>decatriene(Bullvalene)
Joesel, Rainer,Schroeder, Gerhard
, p. 1428 - 1437 (2007/10/02)
Bicyclodecatetraene (1) and bullvalene (8) generate cycloadducts 3 and 9 with N-phenyltriazolinedione (2).Base-induced hydrolysis and subsequent oxidation give tetracyclic and tricyclic azo compounds 6 and 12, respectively. 6 has a half-life of ca.