Issue 15, 1998

Transylidation of a transiently formed nitrilium phosphane ylide complex

Abstract

Thermal decomposition of the 3-phenyl-substituted 2H-azaphosphirene complex 1 in the presence of dimethyl cyanamide and dimethyl acetylenedicarboxylate (DMAD) yielded dimethylamino-substituted products, the 2H-1,2- azaphosphole complex 4b and the diastereoisomeric Δ3-1,3,2-oxazaphospholene complexes 5a,b; this represents the first example of 1,3-dipolar cycloaddition reactions of a nitrilium phosphane ylide complex that is generated in situ by transylidation.

Article information

Article type
Paper

Chem. Commun., 1998, 1529-1530

Transylidation of a transiently formed nitrilium phosphane ylide complex

H. Wilkens, F. Ruthe, P. G. Jones and R. Streubel, Chem. Commun., 1998, 1529 DOI: 10.1039/A802569J

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