John P. Lowe, B. David Silverman
Accounts of Chemical Research
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.
John P. Lowe, B. David Silverman
Accounts of Chemical Research
B. David Silverman
Protein Science
Arthur Greenberg, B. David Silverman
Journal of Organic Chemistry
B. David Silverman
Ecological Modelling