## Abstract Multiple conformational states in heterochiral diproline sequences have been characterized in the solid state by the determination of the crystal structures of seven tripeptides in enantiomeric and racemic forms. The sequences of the type Piv‐^D^Pro‐^L^Pro‐^D^Xxx‐NHMe (__D‐L‐D__) [^D^Xx
Thermodynamics of sublimation, crystal lattice energies, and crystal structures of racemates and enantiomers: (+)- and (±)-ibuprofen
✍ Scribed by German L. Perlovich; Sergey V. Kurkov; Lars Kr. Hansen; Annette Bauer-Brandl
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 195 KB
- Volume
- 93
- Category
- Article
- ISSN
- 0022-3549
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Chiral spirobinaphtopyrans 1-9 were synthesised using the acid catalyzed aldol condensation of 2-hydroxy-1-naphthaldehyde or 1-hydroxy-2-naphthaldehyde with the appropriate ketone and subsequent reaction of the isolated pyrylium salt with base. Separation or enrichment of enantiomers was accomplishe
The crystal structures of three sulfonamides with the general structure 4-NH 2 -C 6 H 4 -SO 2 NH-C 6 H 4/3 -R (R ¼ 4-Et; 4-OMe; 5-Cl-2-Me) have been determined by X-ray diffraction. On the basis of our previous data and the results obtained a comparative analysis of crystal properties was performed: