Allylhydrazones are reported to undergo an elaborate [3,3]-sigmatropic shift/N2 extrusion sequence. Both concerted and radical cation pathways for the [3,3]-sigmatropic shift of several N-allylhydrazones were investigated using B3LYP/6-31+G(d,p) calculations. It was discovered that, assuming facile formation of the N-allylhydrazone radical cation, the rearrangement takes place through a series of low barrier steps energetically preferred to the concerted alternative available to neutral N-allylhydrazones. Subsequent N2 extrusions forming corresponding homoallyl radicals were found to be extremely facile
He rearrangement of a range of N-benzyl-O-allylhydroxylamines to the corresponding N-allylhydroxylam...
N-Allylhydrazones are an extremely useful, but under-explored synthetic intermediate. These compound...
Mechanisms of thermal isomerization of allyl tetrazolyl ethers derived from the carbocyclic allylic ...
The spontaneous rearrangement of allylic azides is thought to be a sigmatropic reaction. Presented h...
The spontaneous rearrangement of allylic azides is thought to be a sigmatropic reaction. Presented h...
The competition between rearrangement of the excited allyl radical via a 1,3 sigmatropic shift versu...
A novel [2,3]-sigmatropic rearrangement whereby N-benzyl-O-allylhydroxylamines undergo transformatio...
The mechanism of the thermal rearrangement of 1-aryl-5-allyloxytetrazoles 1 to give 1-aryl-4-allylte...
A novel [2,3]-sigmatropic rearrangement whereby N-benzyl-O-allylhydroxylamines undergo transformatio...
The intramolecularity of the thermal rearrangement of 1-aryl-5-allyloxy-1H-tetrazoles 1 to 1-aryl-4-...
The mechanisms of [3s,5s]sigmatropic shifts of octa-1,3,7-triene and 7-methylenenona-1.3,8-triene ha...
The mechanisms of [3s,5s]sigmatropic shifts of octa-1,3,7-triene and 7-methylenenona-1.3,8-triene ha...
The intramolecularity of the thermal rearrangement of 1-aryl-5-allyloxy-1H-tetrazoles 1 to 1-aryl-4-...
The rearrangement of a range of N-benzyl-O-allylhydroxylamines to the corresponding N-allylhydroxyla...
The mechanisms of [3s,5s]sigmatropic shifts of octa-1,3,7-triene and 7-methylenenona-1.3,8-triene ha...
He rearrangement of a range of N-benzyl-O-allylhydroxylamines to the corresponding N-allylhydroxylam...
N-Allylhydrazones are an extremely useful, but under-explored synthetic intermediate. These compound...
Mechanisms of thermal isomerization of allyl tetrazolyl ethers derived from the carbocyclic allylic ...
The spontaneous rearrangement of allylic azides is thought to be a sigmatropic reaction. Presented h...
The spontaneous rearrangement of allylic azides is thought to be a sigmatropic reaction. Presented h...
The competition between rearrangement of the excited allyl radical via a 1,3 sigmatropic shift versu...
A novel [2,3]-sigmatropic rearrangement whereby N-benzyl-O-allylhydroxylamines undergo transformatio...
The mechanism of the thermal rearrangement of 1-aryl-5-allyloxytetrazoles 1 to give 1-aryl-4-allylte...
A novel [2,3]-sigmatropic rearrangement whereby N-benzyl-O-allylhydroxylamines undergo transformatio...
The intramolecularity of the thermal rearrangement of 1-aryl-5-allyloxy-1H-tetrazoles 1 to 1-aryl-4-...
The mechanisms of [3s,5s]sigmatropic shifts of octa-1,3,7-triene and 7-methylenenona-1.3,8-triene ha...
The mechanisms of [3s,5s]sigmatropic shifts of octa-1,3,7-triene and 7-methylenenona-1.3,8-triene ha...
The intramolecularity of the thermal rearrangement of 1-aryl-5-allyloxy-1H-tetrazoles 1 to 1-aryl-4-...
The rearrangement of a range of N-benzyl-O-allylhydroxylamines to the corresponding N-allylhydroxyla...
The mechanisms of [3s,5s]sigmatropic shifts of octa-1,3,7-triene and 7-methylenenona-1.3,8-triene ha...
He rearrangement of a range of N-benzyl-O-allylhydroxylamines to the corresponding N-allylhydroxylam...
N-Allylhydrazones are an extremely useful, but under-explored synthetic intermediate. These compound...
Mechanisms of thermal isomerization of allyl tetrazolyl ethers derived from the carbocyclic allylic ...