Description
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
| Date made available | 2005 |
|---|---|
| Publisher | Cambridge Crystallographic Data Centre |
Research output
- 1 Article
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Virtually complete control of simple and face diastereoselectivity in the Michael addition reactions between achiral equivalents of a nucleophilic glycine and (S)- or (R)-3-(E-enoyl)-4-phenyl-1,3-oxazolidin-2-ones: Practical method for preparation of β-substituted pyroglutamic acids and prolines
Soloshonok, V. A., Ueki, H., Tiwari, R., Cai, C. & Hruby, V. J., Jul 23 2004, In: Journal of Organic Chemistry. 69, 15, p. 4984-4990 7 p.Research output: Contribution to journal › Article › peer-review
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