(-)-(R)-5,5-dimethylmorpholinyl-2-acetic acid ethyl ester hydrochloride, C10H20NO3+.Cl-
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
One of the enantiomers of 5,5-dimethylmorpholinyl-2-acetic acid is observed to be a GABAB receptor antagonist. The absolute configuration of the inactive enantiomer is found to be the R configuration. The morpholine ring adopts a chair conformation with the acetic acid moiety in an equatorial position. In the crystal packing, hydrogen bonds are observed between the ammonium group and the chloride ions.
Originalsprog | Engelsk |
---|---|
Tidsskrift | Acta Crystallographica Section C: Crystal Structure Communications |
Vol/bind | 53 |
Udgave nummer | 8 |
Sider (fra-til) | 1088-1091 |
Antal sider | 4 |
ISSN | 0108-2701 |
DOI | |
Status | Udgivet - 15 aug. 1997 |
ID: 382748111