B. David Silverman
Quantitative Structure-Activity Relationships
The molecular structures of the diequatorial and diaxial conformers of the syn- and anti-benzo[c]phenanthrene 'fjord-region' diol epoxide diastereoisomers have been determined by the Allinger force-field program. Certain features of steric crowding in the 'fjord-region' of the molecule that contribute to relative conformer stability are discussed.