| Literature DB >> 12112325 |
Hiroki Takahashi1, Rui Tamura, Daisuke Fujimoto, Zsolt Lepp, Kimiko Kobayashi, Takanori Ushio.
Abstract
Full characterization of the crystal structures of the racemate, nonracemate (20% ee), and pure enantiomer of [2-[4-(3-ethoxy-2-hydroxypropoxy)phenylcarbamoyl]ethyl]trimethylammonium p-bromobenzenesulfonate (NBMe3), which has successfully shown an unusual enantiomeric resolution phenomenon, "preferential enrichment," was achieved by means of X-ray crystallographic analysis and construction of the binary melting point phase diagram. The crystalline nature of the racemate is not a racemic compound but a fairly ordered mixed crystal composed of the two enantiomers. The crystal structure of the nonracemate (20% ee) is virtually identical with that of the racemate and similar to that of the pure enantiomer. The binary melting point phase diagram of NBMe3 is consistent with the nature of a mixed crystal composed of the two enantiomers. Copyright 2002 Wiley-Liss, Inc.Entities:
Mesh:
Year: 2002 PMID: 12112325 DOI: 10.1002/chir.10080
Source DB: PubMed Journal: Chirality ISSN: 0899-0042 Impact factor: 2.437