Abstract
The title compound crystallizes in the monoclinic space group P21/n, with a = 6.225(1), b = 14.612 (1), c = 15.520 (1) Å, β = 96.6(3)°, Z = 4 and V = 1402.4Å3. The stereochemistry of the 7/5-fused ring system is trans, the 7-membered and the 5-membered rings are found to be in the chair and envelope conformations, respectively. This represents the first study of a compound containing the 7/5-ring skeleton shown in (3) below.
| Original language | English |
|---|---|
| Pages (from-to) | 33-38 |
| Number of pages | 6 |
| Journal | Journal of Chemical Crystallography |
| Volume | 29 |
| Issue number | 1 |
| DOIs | |
| State | Published - Jan 1999 |
Bibliographical note
Funding Information:This paper is dedicated to the memory of Professor Elmer. O. Schlemper. In his untimely demise one of us (M.S.H) has not only lost a valued colleague but a true friend indeed. We are also grateful to the KFUPM Chemistry Department and the Research Committee for financial assistance to up-grade the computer system in the CAD4 Diffractometer.
Keywords
- 1,3-dipolar addition
- 7/5-Fused ring system
- Isooxazolidine
ASJC Scopus subject areas
- General Chemistry
- Condensed Matter Physics
Fingerprint
Dive into the research topics of 'The crystal and molecular structure of trans-dimethyl 2α-methyl(3αH) perhydro [1,2]oxazolo-[2,3-a]azepine-2α,3α-dicarboxylate: A 7/5-fused ring system'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver