78414-58-1Relevant academic research and scientific papers
TBHP as Methyl Source under Metal-Free Aerobic Conditions To Synthesize Quinazolin-4(3H)-ones and Quinazolines by Oxidative Amination of C(sp3)–H Bond
Mukhopadhyay, Sushobhan,Barak, Dinesh S.,Batra, Sanjay
supporting information, p. 2784 - 2794 (2018/06/04)
tert-Butyl hydroperoxide (TBHP) served as the methyl source under metal-free aerobic conditions in the oxidative amination of the C(sp3)–H bond to synthesize quinazolin-4(3H)-ones and quinazolines from 2-aminobenzamides and 2-carbonyl-substituted anilines, respectively.
13C Nuclear Magnetic Resonance Spectra of Methoxycyclohexane Derivatives. Rotamer Populations about C-OMe Bonds as indicated by 13C Chemical Shifts of Methoxy- and Ring-carbons and 3JC,H Coupling Constants
Haines, Alan H.,Shandiz, Mohammad Seyedi
, p. 1671 - 1678 (2007/10/02)
Methoxy 13C chemical shifts in methoxycyclohexane derivatives may be rationalized in terms of rotamer populations about the C-OMe bond and δ1-effects caused by steric interaction of the methoxy-group with substituents at the neighbouring 2- and 6-positions.Information on rotamer populations is obtained also from the 13C chemical shifts of C-2 and C-6, and from the three-bond coupling between the proton at C-1 and the methoxy-carbon atom.
