Issue 6, 1999

Dual reaction behaviour of an in situ generated nitrilium phosphane ylide complex towards carbon–sulfur π-systems

Abstract

[3 + 2] Cycloaddition of in situ generated nitrilium phosphane ylide complex 4b with phenylisothiocyanate yielded N-piperidino-substituted Δ3-1,3,2-thiazaphospholene complex 5 regioselectively, whereas with benzyl N,N-dimethyl dithiocarbamate ester the thiaphosphirane 9 is obtained; these reactions, a 1,3-dipolar cycloaddition and a transylidation, shed first light on the reactivity of a nitrilium phosphane ylide complex towards different C,S π-systems.

Article information

Article type
Paper

Chem. Commun., 1999, 499-500

Dual reaction behaviour of an in situ generated nitrilium phosphane ylide complex towards carbon–sulfur π-systems

R. Streubel and C. Neumann, Chem. Commun., 1999, 499 DOI: 10.1039/A809741K

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