The base-induced rearrangement of 1,2,4-oxadiazoles into isoxazoline derivatives is reported. This represents the first example of a three-atom side-chain rearrangement that involves a saturated CCO side chain at C-3 of the oxadiazole. Nonaromatic 3-amino-isoxazoline derivatives are obtained in good yields. Interestingly, this reaction occurs through the rearrangement of aromatic oxadiazoles to form less stable bonds than those that are broken
A method for the conversion of O-propargylic hydroxylamines into 2-isoxazolines in 60-84% yield is d...
Fluoroalkylated 2-ylamino-imidazoles have been synthesized by reaction of 3-amino-5-phenyl-1,2,4-oxa...
A highly chemoselective reaction between 5-aminoisoxazoles and α-diazocarbonyl compounds has been de...
The base-induced rearrangement of 1,2,4-oxadiazoles into isoxazoline derivatives is reported. This r...
The thermal rearrangement of N-1,2,4-oxadiazol-3-yl-hydrazones into 1,2,4-triazole derivatives is re...
A novel base-induced rearrangement of isoxazoles into imidazole derivatives is reported. In the iso...
N-Alkyl substituted oxaziridines undergo a [3+2] cycloaddition reaction with a variety of terminal a...
The experimental investigation of the base-catalyzed rearrangements of 3-acylamino-1,2,4-oxadiazoles...
The thermal rearrangements of 3-acylamino-5-methylisoxazoles 1 have been investigated under basic a...
3-Aryltetrahydrobenzisoxazoles prepared en route to the coleophomone natural products and analogues,...
Acyclic nitrones react with dimethyl acetylenedicarboxylate (DMAD) to give stable isoxazolines, from...
[Figure not available: see fulltext.] 1,2,4-Oxadiazoles are heterocycles characterized by low aromat...
927-9304-(5-Methyl-3-isoxazol yl)-3,5-diaryl -Δ2-1,2,4-oxadiazolines have been prepared by benzoni...
A highly chemoselective reaction between 5-aminoisoxazoles and α-diazocarbonyl compounds has been de...
The unusual migration of a nitro group from the \u3b2- to the \u3b1- position of a \u3b2-aryl-\u3b1-...
A method for the conversion of O-propargylic hydroxylamines into 2-isoxazolines in 60-84% yield is d...
Fluoroalkylated 2-ylamino-imidazoles have been synthesized by reaction of 3-amino-5-phenyl-1,2,4-oxa...
A highly chemoselective reaction between 5-aminoisoxazoles and α-diazocarbonyl compounds has been de...
The base-induced rearrangement of 1,2,4-oxadiazoles into isoxazoline derivatives is reported. This r...
The thermal rearrangement of N-1,2,4-oxadiazol-3-yl-hydrazones into 1,2,4-triazole derivatives is re...
A novel base-induced rearrangement of isoxazoles into imidazole derivatives is reported. In the iso...
N-Alkyl substituted oxaziridines undergo a [3+2] cycloaddition reaction with a variety of terminal a...
The experimental investigation of the base-catalyzed rearrangements of 3-acylamino-1,2,4-oxadiazoles...
The thermal rearrangements of 3-acylamino-5-methylisoxazoles 1 have been investigated under basic a...
3-Aryltetrahydrobenzisoxazoles prepared en route to the coleophomone natural products and analogues,...
Acyclic nitrones react with dimethyl acetylenedicarboxylate (DMAD) to give stable isoxazolines, from...
[Figure not available: see fulltext.] 1,2,4-Oxadiazoles are heterocycles characterized by low aromat...
927-9304-(5-Methyl-3-isoxazol yl)-3,5-diaryl -Δ2-1,2,4-oxadiazolines have been prepared by benzoni...
A highly chemoselective reaction between 5-aminoisoxazoles and α-diazocarbonyl compounds has been de...
The unusual migration of a nitro group from the \u3b2- to the \u3b1- position of a \u3b2-aryl-\u3b1-...
A method for the conversion of O-propargylic hydroxylamines into 2-isoxazolines in 60-84% yield is d...
Fluoroalkylated 2-ylamino-imidazoles have been synthesized by reaction of 3-amino-5-phenyl-1,2,4-oxa...
A highly chemoselective reaction between 5-aminoisoxazoles and α-diazocarbonyl compounds has been de...