ORIGIN OF DIASTEREOSELECTIVITY IN THE NITRILE OXIDE CYCLOADDITIONS WITH OPPOLZERS CHIRAL SULTAMS - COULOMBIC INTERACTION AS THE KEY ROLE INDIASTEREOFACIAL DIFFERENTIATION
Ks. Kim et al., ORIGIN OF DIASTEREOSELECTIVITY IN THE NITRILE OXIDE CYCLOADDITIONS WITH OPPOLZERS CHIRAL SULTAMS - COULOMBIC INTERACTION AS THE KEY ROLE INDIASTEREOFACIAL DIFFERENTIATION, Journal of the American Chemical Society, 115(16), 1993, pp. 7472-7477
Diastereofacial selectivity in the nitrile oxide cycloadditions with O
ppolzer's chiral sultams cannot be explained with the conventional fac
e shielding by sterically bulky groups. To find the origin of the dias
tereoselectivity, the transition states for the cycloadditions have be
en studied with semiempirical quantum mechanical calculations using th
e PM3 method. The calculated product ratios are in good agreement with
experiment. We find that the activation barriers for the favored and
disfavored transition states are strongly correlated with the Coulombi
c repulsions between the dipolar oxygen and the sultam oxygens. Such c
orrelation is also found from ab initio calculations using the PM3 opt
imized geometries. In addition, when two oxygen atoms of the sulfone g
roup in the sultam systems are removed, these isothiazolidine systems
have very small energy differences between the top-facial and bottom-f
acial transition states, showing no diastereoselectivity. Therefore, w
e suggest that the electrostatic effect is a main factor governing the
diastereofacial selectivity for the sultam systems. These systems can
be considered as one of the most typical case of Hehre's claim that t
he electrostatic effect is a very general determinant of pi-facial sel
ectivity.