๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

2,2-Versus 2,6-dialkylation of the pyrrolidine enamine of 2-methylcyclohexanone with electrophilic olefins

โœ Scribed by Firrell, N. F.; Hickmott, P. W.

Book ID
121653315
Publisher
Royal Society of Chemistry
Year
1969
Weight
245 KB
Volume
10
Category
Article
ISSN
0577-6171

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Chemistry of enamines II The structure o
Chemistry of enamines II The structure of the pyrrolidine enamine of 2-methylcyclohexanone
โœ Sudarshan K. Malhotra; Francis Johnson ๐Ÿ“‚ Article ๐Ÿ“… 1965 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 253 KB

The position isomer (I), having a trisubstituted double bond was originally assigned by Stork and associates to the structure of the pyrrolidine enamine of a substituted cyclohexanone. The tetrasubstituted ethylenic isomer II which was excluded on the basis of N.M.R. spectrum, involves steric interf

1,2-cyanoselenenylation of olefins. Reac
1,2-cyanoselenenylation of olefins. Reaction of enamines with phenyl selenocyanate
โœ Shuji Tomoda; Yoshito Takeuchi; Yujiro Nomura ๐Ÿ“‚ Article ๐Ÿ“… 1982 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 256 KB

The first 1,2-cyanoselenenylatlon of carbon-carbon double bond has been achieved by the reaction of SIX enamlnes derived from ketones or aldehydes with phenyl selenocyanate in ethanol. The products, 2-phenylseleno-1-amlnocarbonltrlles, were obtalned In al-98% yield with complete reglo-and stereospec