The effect of the nitrogen function of 4-ketodecahydroquinoline on the relative stability of cis and trans isomers
作者： �. A. Mistryukov , V. F. Kicherov
DOI: 10.1007/BF01118765
关键词:
摘要: 1. The most stable isomers of the bases or hydrochlorides decahydro-4-quinolone and N-benzoyldecahydro4-qulnolone belong to different groups with respect linking rings. 2. We suggest need review stereochemical determinations Huckel for cis trans decahydroquinolines.
springer.com
sci-hub.se 参考文章(4)
Walter Hückel, Friedrich Stepf, Zur Stereochemie bicyclischer Ringsysteme. IV. Die Stereoisomerie des Dekahydrochinolins Justus Liebig's Annalen der Chemie. ,vol. 453, pp. 163- 176 ,(1927) , 10.1002/JLAC.19274530111
J. McKenna, A. Tulley, 198. Stereochemical investigations of cyclic bases. Part V. Exhaustive methylation of N-methyl-4-aza-5α- and -5β-cholestane, and the reaction of the methines with acetic acid: the possibility of “α′β” Hofmann elimination with cyclic ammonium hydroxides Journal of The Chemical Society (resumed). pp. 945- 952 ,(1960) , 10.1039/JR9600000945
F. Galinovsky, G. Bianchetti, O. Vogl, Über die Racemisierung des isopelletierins und methylisopelletierins Monatshefte Fur Chemie. ,vol. 84, pp. 1221- 1227 ,(1953) , 10.1007/BF00904147
A. R. H. Cole, R. Norman Jones, Konrad Dobriner, A Relationship between the Stereochemical Configuration of 3-Hydroxysteroids and their Infrared Absorption Spectra1 Journal of the American Chemical Society. ,vol. 74, pp. 5571- 5575 ,(1952) , 10.1021/JA01142A006