185380-16-9Relevant articles and documents
?-Face selectivities in nucleophilic additions to 2-endo-arylnorbornan-7-ones: the role of through-space electrostatic interactions
Mehta, Goverdhan,Khan, Faiz Ahmed,Mohal, Narinder,Namboothiri, I. N. Narayan,Kalyanaraman, P.,Chandrasekhar, Jayaraman
, p. 2665 - 2668 (2007/10/03)
Experimental diastereoselectivities in hydride reduction of 2-endo-arylnorbornan-7-ones and computed transition state energetics reveal that the facial selectivity in these systems is predominantly determined by repulsions between the approaching nucleoph