Werner Baechtold, Willi Kotyczka, et al.
IEEE T-MTT
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.
Werner Baechtold, Willi Kotyczka, et al.
IEEE T-MTT
Bo Wen, Julia Liu, et al.
DREAM 2024
Zhiguo Li, Jorma Toppari, et al.
AMIA Annual Symposium 2021
Diwakar Mahajan, Jennifer J. Liang, et al.
Journal of Biomedical Informatics