David C. Spellmeyer, William C. Swope
Perspectives in Drug Discovery and Design
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.
David C. Spellmeyer, William C. Swope
Perspectives in Drug Discovery and Design
G. Bryan Street, W.D. Gill, et al.
Journal of the Chemical Society, Chemical Communications
Jannis Born, Matteo Manica
ICLR 2022
Vesna Barros, Tal Tlusty, et al.
Radiology