The structure of enamines of 2-substituted ketones
โ Scribed by William D. Gurowitz; Madeline A. Joseph
- Publisher
- Elsevier Science
- Year
- 1965
- Tongue
- French
- Weight
- 271 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0040-4039
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Methods for deuterating orpjanic rsolecules have becceba increasinkly important in recentyearsbecause of the existing interest inmechanistic aspects of organic reactions, includin~decipberingofmassspectrsliragmentatlon p&terns. The susceptibility of ensminestoelectrophllicattack(1) suggested that th
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