作者:Alois H. A. Tinnemans、Wim H. Laarhoven
DOI:10.1039/p29760001104
日期:——
Several new diarylbutenynes have been synthesized and analyses of the n.m.r. and u.v. spectra are described. For planar trans-isomers a conformational preference was found for 1-(α-naphthyl)- but not for 1-(β-naphthyl)-4-arylbutenynes. This difference is also found between compounds with C-1 attached to the α- or β-position of a larger aryl group.
已经合成了几种新的二芳基丁烯炔,并描述了nmr和uv光谱的分析。对于平面反式异构体,发现构型偏爱于1-(α-萘基)-,而不是1-(β-萘基)-4-芳基丁烯。在C-1连接到较大芳基的α-或β-位置的化合物之间也发现了这种差异。