Organophosphorus compounds; 142: A simple approach to 1,2,4-selena- and telluradiphospholes from phosphaalkynes and the chalcogen elements and a first study of their reactivity
Smf. Asmus et al., Organophosphorus compounds; 142: A simple approach to 1,2,4-selena- and telluradiphospholes from phosphaalkynes and the chalcogen elements and a first study of their reactivity, SYNTHESIS-S, (9), 1999, pp. 1642-1650
Phosphaalkynes 3 react with elemental selenium or tellurium to furnish the
1,2,4-selena- (5) or 1,2,4-tellutadiphospholes (15), respectively. Although
the telluradiphuspholes 15 do not exhibit any selective cycloaddition reac
tivity, two equivalents of the phosphaalkyne 3 do undergo cycloaddition to
the selenadiphospholes 5 through a [4+2]/[2+2+2] sequence to afford the tet
racyclic products 8. The crystal structure of compound 80 has been determin
ed, This cage compound is alkylated at P-4 on reaction with methyl trifluor
omethanesulfonate to give 10 while selenium and sulfur react at P-7 of 8 to
afford 11a,b. Compound 80 reacts with bromine by way of P/P bond cleavage
and an unexpected rearrangement to furnish another tetracyclic compound 12
with a novel structure that has been confirmed by X-ray crystallography.