✍ Scribed by P Van Hecke; H.W Spiess; U Haeberlen; S Haussühl
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract ^19^F and ^1^H NMR spectra of the products of nucleophilic attack on octafluoroindene are analysed and structures assigned. The major product in the reaction of butyllithium with octafluoroindene is 3‐methylheptafluoroindene, with sodium borohydride it is 2‐hydroheptafluoroindene and wi
Interactions between polar groups and zc systems were studied for stacked aryls in l-fluorophenyl-8arylnaphthalenes, in which an 'electron-rich' aryl ring is forced in a stacked geometry with an 'electron-poor' fluorophenyl ring; the rotation process was examined using different NMR techniques (line
## Abstract Novel 2‐acetylamino‐4‐acetyl‐5‐aryl(heteryl)‐1,3,4‐thiadiazolines, 2‐acetylamino‐5‐aryl(heteryl)‐1,3,4‐thiadiazoles, and some of their salts were prepared and studied by multinuclear ^1^H, ^13^C, ^15^N, ^19^F and 2D NMR spectroscopy. The acetylation of thiosemicarbazones is accompanied