Strong evidence for stereoselective 1,3-additions of transient nitrilium phosphane-ylide complexes: synthesis of the first 1-aza-3-phosphabuta-1,3-diene complexes
R. Streubel et al., Strong evidence for stereoselective 1,3-additions of transient nitrilium phosphane-ylide complexes: synthesis of the first 1-aza-3-phosphabuta-1,3-diene complexes, CHEM COMMUN, (15), 2001, pp. 1334-1335
Synthesis of the first 1-aza-3-phosphabuta-1,3-diene complexes was achieved
by heating solutions of 2H-azaphosphirene tungsten complexes, 1-piperidino
nitrile and [bis(trimethylsilyl)methylene]chlorophosphane; X-ray structure
analysis of one new complex revealed a cisoid position of the chlorine atom
and the phosphaalkene unit at the C,N,P-core of the trapped nitrilium phos
phane-ylide complex and a distorted heterobutadiene pi -system.