85342-80-9Relevant academic research and scientific papers
UNTERSUCHUNGEN ZUR STRUKTUR UND STEREOCHEMIE DER ADDITIONSPRODUKTE VON NUKLEOPHILEN AN VON N-METHYLBENZIMIDCHLORID ABGELEITETE CARBENCHELATKOMPLEXE
Brunner, Henri,Wachter, Joachim,Bernal, Ivan,Reisner, George M.,Benn, Reinhard
, p. 179 - 190 (1983)
In the reaction of (I) with C6H5MgBr the phenyl group adds to the carbene carbon atom giving the neutral complex (V).V crystallizes in the space group P21/c with the cell constants a 11.803(5), b 12.114(6), c 17.198(6) Angstroem, β 96.61(3)0, V 2431.2 Angstroem3, Z = 4, ρcalc 1.45 g cm-3.For 2979 reflections the R value is 5.1, Rw = 4.8.The stereoisomers IIIA and IIIB, formed in the H- addition to I, are 1H NMR spectroscopically investigated by means of Nuclear-Overhauser-Effect Difference Spectroscopy in order to elucidate the orientation of the incoming H substituent with respect to the C5H5 group.
