✍ Scribed by Shuntaro Mataka; Masashi Tashiro; Osamu Misumi; Wei Hua Lin; Kazufumi Takahashi; Akiyoshi Tori-i
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Correlation analysis of the oxidation potentials of a series of N,N',N@-triphenyl-1,3,5-triaminobenzenes (TPABs) substituted at the para positions of the outer phenyl rings shows a linear free energy relationship with resonance-enhanced substituent parameters (s ). Reaction parameters (r ) for oxida
## Abstract The complete ^1^H and ^13^C NMR spectral assignments of seven positional isomers of __N__,__N__‐dimethylsulfamoylquinolines 2–8 and quinoline have been made using 1D and 2D NMR techniques, including COSY, HMQC and HMBC experiments. Δδ~H~ and Δδ~C~ substituent effects induced by the sulf
## Abstract __N__,__N__‐diisopropylamides and ‐thioamides show hindered rotation around the NCH bonds, and the presence of mixtures of conformational isomers can be demonstrated at temperatures below 273 K in solution. ^1^H and ^13^C NMR spectra of these conformers are measured and assigned. The ^