129302-84-7Relevant academic research and scientific papers
13C, 1H Spin-Spin Coupling. X - Norbornane: A Reinvestigation of the Karplus Curve for 3J(13C, 1H)
Aydin, Rafet,Guenther, Harald
, p. 448 - 457 (1990)
13C, 1H spin-spin coupling constants over one, two and three bonds were measured from the 100 MHz 13C NMR spectra of deuteriated isotopomers of norbornane-d1 (1) and fenchane-2-d1 (2) and also of a number of monodeuteriated alkyl-substituted adamantanes.The magnitudes of the corresponding J(13C, 1H) values derived from these data by application of the well known relationship J(X, 1H) = 6.5144J(X, 2H) are discussed with respect to the structural data for the hydrocarbons, which were taken from force field calculations with the Allinger MM2 method.In particular, the dihedral angle dependence and the Karplus curve for 3J(13C, 1H) are investigated.Coupling constants calculated by the FP-INDO method are compared with the experimental data, and the effect of substitution by additional CC bonds in α-, β- and γ-positions of the 13C-α-C-β-C-γ-H bond fragment is elucidated.If substituent effects that arise through branching and methyl substitution in 1 and 2 are taken into account for dihedral angles Φ > 90 deg, one derives 3J(13C, 1H) = 4.50 - 0.87 cos Φ + 4.03 cos 2Φ with J(0 deg) = 7.7, J(60 deg) = 2.0 and J(180 deg) = 9.4 Hz.
Room-Temperature Palladium-Catalyzed Deuterogenolysis of Carbon Oxygen Bonds towards Deuterated Pharmaceuticals
Ou, Wei,Xiang, Xudong,Zou, Ru,Xu, Qing,Loh, Kian Ping,Su, Chenliang
supporting information, p. 6357 - 6361 (2021/02/16)
Site-specific incorporation of deuterium into drug molecules to study and improve their biological properties is crucial for drug discovery and development. Herein, we describe a palladium-catalyzed room-temperature deuterogenolysis of carbon–oxygen bonds
