145147-08-6Relevant academic research and scientific papers
Chemistry of N-Nitroso Compounds. 1. Synthesis and Stereodynamics of N-Nitrosopiperidines and N-Nitrosopiperidin-4-ones
Ravindran, Thiruvenkadam,Jeyaraman, Ramasubbu,Murray, Robert W.,Singh, Megh
, p. 4833 - 4840 (1991)
The stereochemistry of a series of N-nitroso-r-2,c-6-diphenylpiperidin-4-ones (10-15) and N-nitroso-r-2,c-6-diphenylpiperidines (16-18) in solution has been investigated by 1H NMR, 13C NMR, and dynamic 1H NMR spectroscopic studies.Unlike the r-2,c-6-dialkyl-N-nitrosopiperidines, which have diaxial alkyl groups, these N-nitroso-r-2,c-6-diphenylpiperidines (16-18) and N-nitroso-r-2,c-6-diphenylpiperidin-4-ones (10-15) have diequatorial phenyl groups even though the nitroso group is coplanar to the dynamically averaged plane of the piperidine ring.The rotamer populations of the N-NO orientations in the nitrosamines were derived from continuous wave 1H NMR spectral data and are correlated with the steric bulk of the substituents present at the C-3 and C-5 positions.N-Nitroso-r-2,c-6-diphenylpiperidine-4-one (10) was found to have a higher rotational barrier than N-nitroso-r-2,c-6-diphenylpiperidine (16).We attribute this difference to a greater degree of coplanarity (C3-C2-N1-C6-C5) in 10 than in 16.The rotational barriers in 10 were found to decrease as the bulk of the substituents at C3 and C5 increased.The rotational barrier in N-nitroso-r-2,c-6-diphenylpiperidine (16) was found to be lower than the reported rotational barriers of N-nitroso-r-2,c-6-dimethylpiperidine and N-nitroso-2,2,6,6-tetramethylpiperidine.
PHARMACEUTICALLY ACTIVE COMPOUNDS AND METHODS OF USE
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, (2008/06/13)
The present invention relates to certain imine-substituted heterocyclic compounds, and methods of treatment and pharmaceutical compositions that utilize or comprise one or more such compounds. Compounds of the invention are particularly useful for the tre
