M. Pitman, W.K. Huber, et al.
J. Comput. Aided Mol. Des.
The relative stabilities of conformers of the syn and anti-diastereomers of the fjord and bay-region diol-epoxides of benzo(c)phenanthrene (BCP) and benzo(a)anthracene (BA) have been calculated. Steric crowding in the fjord-region of BCP is shown to stabilize the syn-diequatorial and anti-diaxial conformers of BCP. In contrast, the most stable conformers of the bay-epoxides of BA are found to be the syn-diaxial and anti-diequatorial.
M. Pitman, W.K. Huber, et al.
J. Comput. Aided Mol. Des.
Qihua Wang, Hongxia Jin
ICHI 2011
G. Bryan Street, W.D. Gill, et al.
Journal of the Chemical Society, Chemical Communications
Uri Kartoun
Transplantation