Alkyl‐ or Aryl‐Monosubstituted 1,2,3‐Triazoles

The reactions of alkynes and a-nitro-olefines with methylazide and phenylazide was studied. In contrast to known reactions with alkynes which are non-regioselective, methylazide and phenylazide react regiospecifically with a-nitro-olefines and give only one type of triazole after elimination of HN02. These reactions are very useful synthetic approaches to 1,2,3 triazoles.Les 1,2,3 triazoles ont fait I'objet de nombreux

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Alkyl‐ or Aryl‐Monosubstituted 1,2,3‐Triazoles

Cited by 10 publications

References 73 publications

Synthesis of 5‐Diazomethyl Substituted V‐Triazolo [4,5‐D] Pyrimidines

Synthesis of 5‐Diazomethyl Substituted V‐Triazolo [4,5‐D] Pyrimidines

On the Tautomeric Structure of 5‐hydroxy‐ and 5‐mercapto‐1H‐1,2,3‐triazoles: ⁻¹³C NMR analysis

Réactions des Méthylazide et Phénylazide Avec Quelques Alcynes et Oléfines α‐Nitrées. Synthèse Régiospécifique des 1,2,3 Triazoles

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Alkyl‐ or Aryl‐Monosubstituted 1,2,3‐Triazoles

Cited by 10 publications

References 73 publications

Synthesis of 5‐Diazomethyl Substituted V‐Triazolo [4,5‐D] Pyrimidines

Synthesis of 5‐Diazomethyl Substituted V‐Triazolo [4,5‐D] Pyrimidines

On the Tautomeric Structure of 5‐hydroxy‐ and 5‐mercapto‐1H‐1,2,3‐triazoles: −13C NMR analysis

Réactions des Méthylazide et Phénylazide Avec Quelques Alcynes et Oléfines α‐Nitrées. Synthèse Régiospécifique des 1,2,3 Triazoles

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On the Tautomeric Structure of 5‐hydroxy‐ and 5‐mercapto‐1H‐1,2,3‐triazoles: ⁻¹³C NMR analysis