Add to ORKGThe present investigation is concerned with the determination and interpretation of the solvolytic reactivities of nortricyclyl (I), endo-dehydronorbornyl (II), exo-dehydronorbornyl (III), endonorbornyl (IV) and exo-norbornyl (V) halides. This series of structurally similar compounds provides an almost unique opportunity to observe the relationship between stereochemistry and solvolytic reactivities in alicyclic halides
A rationalization of the known difference between the (3,4)J(C4H1) and (3,4)J(C1H4) couplings transm...
A rationalization of the known difference between the (3,4)J(C4H1) and (3,4)J(C1H4) couplings transm...
The ortho-effect of substituents upon the kinetics of reactions taking place at a reaction center at...
The present investigation is concerned with the determination and interpretation of the solvolytic r...
In a previous paper, we reported solvolytic reactivities in 80% ethanol-20% water (by volume) of nor...
In a previous paper, we reported solvolytic reactivities in 80% ethanol-20% water (by volume) of nor...
The buffered trifluoroethanolyses and acetolyses of exo-(2-D)- (6) and endo-(2-D)-5-norbornen-2-yl b...
Despite numerous comparisons of the reactivities of saturated organic halides toward nucleophilic re...
Despite numerous comparisons of the reactivities of saturated organic halides toward nucleophilic re...
I. A review of carbonium-ion reactions of bornyl and norbornyl derivatives involving non-classic...
Fragmentation of (S)-endo-5-norbornenyl-2-oxychlorocarbene [(S)-8] in cyclohexane-d12 gives approxim...
In continuation of earlier work on the effect of structure on reactivity in the norbornyl system a s...
In continuation of earlier work on the effect of structure on reactivity in the norbornyl system a s...
A rationalization of the known difference between the (3,4)J(C4H1) and (3,4)J(C1H4) couplings transm...
A rationalization of the known difference between the (3,4)J(C4H1) and (3,4)J(C1H4) couplings transm...
A rationalization of the known difference between the (3,4)J(C4H1) and (3,4)J(C1H4) couplings transm...
A rationalization of the known difference between the (3,4)J(C4H1) and (3,4)J(C1H4) couplings transm...
The ortho-effect of substituents upon the kinetics of reactions taking place at a reaction center at...
The present investigation is concerned with the determination and interpretation of the solvolytic r...
In a previous paper, we reported solvolytic reactivities in 80% ethanol-20% water (by volume) of nor...
In a previous paper, we reported solvolytic reactivities in 80% ethanol-20% water (by volume) of nor...
The buffered trifluoroethanolyses and acetolyses of exo-(2-D)- (6) and endo-(2-D)-5-norbornen-2-yl b...
Despite numerous comparisons of the reactivities of saturated organic halides toward nucleophilic re...
Despite numerous comparisons of the reactivities of saturated organic halides toward nucleophilic re...
I. A review of carbonium-ion reactions of bornyl and norbornyl derivatives involving non-classic...
Fragmentation of (S)-endo-5-norbornenyl-2-oxychlorocarbene [(S)-8] in cyclohexane-d12 gives approxim...
In continuation of earlier work on the effect of structure on reactivity in the norbornyl system a s...
In continuation of earlier work on the effect of structure on reactivity in the norbornyl system a s...
A rationalization of the known difference between the (3,4)J(C4H1) and (3,4)J(C1H4) couplings transm...
A rationalization of the known difference between the (3,4)J(C4H1) and (3,4)J(C1H4) couplings transm...
A rationalization of the known difference between the (3,4)J(C4H1) and (3,4)J(C1H4) couplings transm...
A rationalization of the known difference between the (3,4)J(C4H1) and (3,4)J(C1H4) couplings transm...
The ortho-effect of substituents upon the kinetics of reactions taking place at a reaction center at...