Among the racemic 2.6-piperidinediones 1-6, compound 6 has the highest anesthetic activity. The enantiomers of 1, 2 , 4 and 5 possess different anesthetic potencies depending on the nature of the aliphatic side chain. The S(-)-enantiomen of the piperidinediones 2, 3 and 5 cause initial CNS stimulati
β¦ LIBER β¦
2,6-Piperidinediones, II. Absolute Configuration of the Enantiomers of 3,3-Disubstituted 2,6-Piperidinediones
β Scribed by Joachim Knabe; Dirk Reischig
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 230 KB
- Volume
- 317
- Category
- Article
- ISSN
- 0365-6233
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Piperidinediones, III. Structure-Activit
β
Joachim Knabe; Horst P. BΓΌch; Dirk Reischig
π
Article
π
1984
π
John Wiley and Sons
π
English
β 255 KB
π 1 views
The Absolute Configuration of (β)-threo-
β
Dr. H. Brockmann jr.; D. MΓΌller-Enoch
π
Article
π
1968
π
John Wiley and Sons
π
English
β 234 KB
π 2 views
ChemInform Abstract: Stereoselective Syn
β
David J. Aldous; William M. Dutton; Patrick G. Steel
π
Article
π
2010
π
John Wiley and Sons
β 27 KB
ChemInform Abstract: Synthesis of Novel
β
K. Srinivas; B. Narsaiah; P. Shanthan Rao; J. Madhusudana Rao
π
Article
π
2010
π
John Wiley and Sons
β 28 KB
Chiral resolution and absolute configura
β
Ornella Azzolina; Vittorio Dal Piaz; Simona Collina; Maria Paola Giovannoni; Car
π
Article
π
1997
π
John Wiley and Sons
π
English
β 96 KB
π 2 views
In a series of 5-acyl-6-phenyl-2,4-substituted-3(2H)-pyridaziones the derivative 1a, with a sulfur stereogenic center, had the most potent activity as human platelet aggregation inhibitor. The resolution of rac-1a was successfully performed by chiral chromatography on Chiralcel OD-R, OD-H, and Chira
ChemInform Abstract: Crystal Structures
β
S. HAUGE; V. JANICKIS; K. MAROEY
π
Article
π
2010
π
John Wiley and Sons
β 33 KB
π 1 views