1-Alkyl-1,2,4-triazinium Ylides as 1,3-Dipoles in a Cycloaddition Reaction with Diethyl Acetylenedicarboxylate

1-Alkyl-1,2,4-triazinium Ylides as 1,3-Dipoles in a Cycloaddition Reaction with Diethyl Acetylenedicarboxylate

Deprotonation of 1-alkyl-5-phenyl-1,2,4-triazinium salts by triethylamine results in the formation of azomethyne ylides which undergo a 1,3-dipolar cycloaddition reaction with diethyl acetylenedicarboxylate to yield pyrrolo[2,1- f]1,2,4-triazines

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Veröffentlicht in:Mendeleev communications 1992, Vol.2 (3), p.85-86
Hauptverfasser: Chupakhin, Oleg N., Rudakov, Boris V., Alexeev, Sergei G., Shorshnev, Sergei V., Charushin, Valerii N.
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container_end_page 86
container_issue 3
container_start_page 85
container_title Mendeleev communications
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creator Chupakhin, Oleg N.
Rudakov, Boris V.
Alexeev, Sergei G.
Shorshnev, Sergei V.
Charushin, Valerii N.
description Deprotonation of 1-alkyl-5-phenyl-1,2,4-triazinium salts by triethylamine results in the formation of azomethyne ylides which undergo a 1,3-dipolar cycloaddition reaction with diethyl acetylenedicarboxylate to yield pyrrolo[2,1- f]1,2,4-triazines
doi_str_mv 10.1070/MC1992v002n03ABEH000144
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title 1-Alkyl-1,2,4-triazinium Ylides as 1,3-Dipoles in a Cycloaddition Reaction with Diethyl Acetylenedicarboxylate
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