Highly functionalized b-aminocyclohexanecarboxylate regio- and stereoisomers were synthesized from a bicyclic b-lactam by successive regioselective iodolactonization, stereo- and regioselective nitrile oxide cycloaddition, lactone ring-opening and isoxazoline ring-openin
The definitive version may be found at www.wiley.comThe reactions of nitrile oxides with monosubstit...
Various [3+2] dipolar cycloadditions were performed using cyclohexenes with basic substituents and n...
Selective functionalizations of the ring olefin bond of various commercial cyclodienes through nitr...
Highly functionalized b-aminocyclohexanecarboxylate regio- and stereoisomers were synthetized from ...
1,3-Dipolar cycloadditions are a versatile method for the formation of five membered heterocyclic ri...
A rapid and simple procedure was devised for the synthesis of multifunctionalized cyclic β-amino est...
A completely regioselective approach to bicyclic isoxazolines has been found starting from 4-cyclope...
Nitrile oxides are highly reactive, but often unstable, compounds that can be used to substitute for...
The scope and stereoselectivity of the acid-promoted cyclization of new tryptophan-based α-amino nit...
A stereocontrolled approach to functionalized acyclic b2,3-amino acid derivatives was accomplished f...
This is the author's peer-reviewed final manuscript, as accepted by the publisher. The published art...
The 1,3-dipolar cycloaddition of nitrile oxides to 1-cyanoenamines gives 5-aminoisoxazoles regiosele...
The cycloaddition of the chiral nitrile oxide 1 to 1-R-substituted 3,3-methylene-5,5-dimethyl-2-pyrr...
A novel intermolecular nitrile oxide cycloaddition sequence has been developed for the formation of ...
Copyright to ElsevierThe 1,3-dipolar cycloaddition of nitrile oxides, generated from aldoximes and n...
The definitive version may be found at www.wiley.comThe reactions of nitrile oxides with monosubstit...
Various [3+2] dipolar cycloadditions were performed using cyclohexenes with basic substituents and n...
Selective functionalizations of the ring olefin bond of various commercial cyclodienes through nitr...
Highly functionalized b-aminocyclohexanecarboxylate regio- and stereoisomers were synthetized from ...
1,3-Dipolar cycloadditions are a versatile method for the formation of five membered heterocyclic ri...
A rapid and simple procedure was devised for the synthesis of multifunctionalized cyclic β-amino est...
A completely regioselective approach to bicyclic isoxazolines has been found starting from 4-cyclope...
Nitrile oxides are highly reactive, but often unstable, compounds that can be used to substitute for...
The scope and stereoselectivity of the acid-promoted cyclization of new tryptophan-based α-amino nit...
A stereocontrolled approach to functionalized acyclic b2,3-amino acid derivatives was accomplished f...
This is the author's peer-reviewed final manuscript, as accepted by the publisher. The published art...
The 1,3-dipolar cycloaddition of nitrile oxides to 1-cyanoenamines gives 5-aminoisoxazoles regiosele...
The cycloaddition of the chiral nitrile oxide 1 to 1-R-substituted 3,3-methylene-5,5-dimethyl-2-pyrr...
A novel intermolecular nitrile oxide cycloaddition sequence has been developed for the formation of ...
Copyright to ElsevierThe 1,3-dipolar cycloaddition of nitrile oxides, generated from aldoximes and n...
The definitive version may be found at www.wiley.comThe reactions of nitrile oxides with monosubstit...
Various [3+2] dipolar cycloadditions were performed using cyclohexenes with basic substituents and n...
Selective functionalizations of the ring olefin bond of various commercial cyclodienes through nitr...
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