6954-16-1Relevant academic research and scientific papers
One-step for the preparation of α-haloacetal of ketones with N-bromosuccinimide/N-chlorosuccinimide (NBS/NCS) and ethylene glycol
Zheng, Zubiao,Han, Bingbing,Wu, Fang,Shi, Tengfei,Liu, Jie,Zhang, Yong,Hao, Jialong
, p. 7738 - 7743 (2016/11/17)
A new process that could directly prepare α-haloacetal of ketones from various ketones with N-halosuccinimide (NBS/NCS) and ethylene glycol in one step without any other catalysts was reported. The effects of solvents, NBS/NCS and reaction temperature were investigated. Under the optimal condition, most of α-haloacetals of ketones were obtained in 90–100% yield.
The Conformational Behaviour of 10-Substituted Spirodecanes
Wolff, J. Jens,Frenking, Gernot,Harms, Klaus
, p. 551 - 561 (2007/10/02)
The conformational behaviour of 10-X-substituted 1,4-dioxa- and 1,4,6-trioxaspirodecanes 1-4 has been studied by 13C-, 19F- and 1H-NMR spectroscopy.Two X-ray analyses of (2a,e) are presented, and their implications to cleavage reactions of chiral acetals are discussed.Participation of twist boat forms in the conformeric equilibrium of at least 1c has been made plausible by observing 13C, 19F-NMR coupling constants.The ratios of axial to equatorial conformers in 1-4 have been calculated by molecular mechanics.
STEREOCHEMICAL STUDIES-XXVI CONFORMATIONAL EQUILIBRIA OF KETALS OF 2-SUBSTITUTED CYCLOHEXANONES
Mursakulov, Ismail G.,Guseinov, M. M.,Kasumov, N. K.,Zefirov, Nikolai S.,Samoshin, V. V.,Chalenko, E. G.
, p. 2213 - 2220 (2007/10/02)
The positions of the conformational equilibria in a series of 2-substituted cyclohexanone ketals have been determined by 1H NMR.For the ethylene ketals 6 the equatorial conformer has been found to be enthalpically preferred.The other ketal syst
