Tannert, René, Schürmann, Markus, Preut, Hans, Arndt, Hans-Dieter, Waldmann, Herbert (2007) (S)-3-[(R)-2,4-Dimethylpent-4-enoyl]-4-isopropyl-5,5-diphenyl-1,3-oxazolidin-2-one. Acta Crystallographica Section E Structure Reports Online, 63 (11) doi:10.1107/s1600536807050295
| Reference Type | Journal (article/letter/editorial) | ||
|---|---|---|---|
| Title | (S)-3-[(R)-2,4-Dimethylpent-4-enoyl]-4-isopropyl-5,5-diphenyl-1,3-oxazolidin-2-one | ||
| Journal | Acta Crystallographica Section E Structure Reports Online | ||
| Authors | Tannert, René | Author | |
| Schürmann, Markus | Author | ||
| Preut, Hans | Author | ||
| Arndt, Hans-Dieter | Author | ||
| Waldmann, Herbert | Author | ||
| Year | 2007 (November 1) | Volume | 63 |
| Issue | 11 | ||
| Publisher | International Union of Crystallography (IUCr) | ||
| DOI | doi:10.1107/s1600536807050295Search in ResearchGate | ||
| Generate Citation Formats | |||
| Mindat Ref. ID | 467299 | Long-form Identifier | mindat:1:5:467299:3 |
| GUID | 0 | ||
| Full Reference | Tannert, René, Schürmann, Markus, Preut, Hans, Arndt, Hans-Dieter, Waldmann, Herbert (2007) (S)-3-[(R)-2,4-Dimethylpent-4-enoyl]-4-isopropyl-5,5-diphenyl-1,3-oxazolidin-2-one. Acta Crystallographica Section E Structure Reports Online, 63 (11) doi:10.1107/s1600536807050295 | ||
| Plain Text | Tannert, René, Schürmann, Markus, Preut, Hans, Arndt, Hans-Dieter, Waldmann, Herbert (2007) (S)-3-[(R)-2,4-Dimethylpent-4-enoyl]-4-isopropyl-5,5-diphenyl-1,3-oxazolidin-2-one. Acta Crystallographica Section E Structure Reports Online, 63 (11) doi:10.1107/s1600536807050295 | ||
| In | (2007, November) Acta Crystallographica Section E Structure Reports Online Vol. 63 (11) International Union of Crystallography (IUCr) | ||
| Abstract/Notes | The title compound, C25H29NO3, was prepared in the course of the generation of depsipeptide libraries resembling the Jasplakinolide family of natural products. The dihedral angle between the phenyl ring planes is 74.1 (3)° The oxazolidinone ring adopts a slightly distorted 4 E conformation with an axial projection of the isopropyl substituent, which is easily rationalized by pseudo-allylic strain exerted by the exocyclic imide carbonyl. The two carbonyl groups adopt a noncolinear S-shaped conformation. | ||
See Also
These are possibly similar items as determined by title/reference text matching only.
