56956-53-7Relevant academic research and scientific papers
Intramolecular cation-π interactions control the conformation of nonrestricted (phenylalkyl)pyridines
Richter, Isabella,Minari, Jusaku,Axe, Philip,Lowe, John P.,James, Tony D.,Sakurai, Kazuo,Bull, Steven D.,Fossey, John S.
, p. 1082 - 1084 (2008/12/20)
NOEsy and fluorescence spectroscopy reveal that conversion of conformationally flexible (phenylalkyl)pyridines into their corresponding N-methyl-pyridinium iodides results in intramolecular π-stacking. The Royal Society of Chemistry.
Intramolecular aromatic alkylation. 28. Synthesis and pharmacological testing of homologized and hydroxylated 3,4-dihydro-1'-methylspiro[naphthalin-1(2H),4'-piperidine
Reimann,Speckbacher,Schuenemann
, p. 35 - 39 (2007/10/02)
The compounds 4, 8, and 10, prepared by standard methods, are converted to the phenylpyridylakanes 9; their methoiodides 11 are reduced to yield the tetrahydropyridines 12. Whereas the cyclisation of 12a gives the isomers 1f and 1g, 12b furnishes only the
