Asymmetric synthesis with chiral hydroxylamines. Synthesis of optically pure 4-substituted azetidinones
Publication
, Journal Article
Baldwin, SW; Aubé, J
Published in: Tetrahedron Letters
January 1, 1987
The reaction between β-substituted acrylate esters and α-methylbenzyl hydroxyl amine affords diastereoisomeric 5-isoxazolidinones, convenient precursors of simple optically pure 2-azetidinones. © 1987.
Duke Scholars
Published In
Tetrahedron Letters
DOI
ISSN
0040-4039
Publication Date
January 1, 1987
Volume
28
Issue
2
Start / End Page
179 / 182
Related Subject Headings
- Organic Chemistry
- 0305 Organic Chemistry
- 0304 Medicinal and Biomolecular Chemistry
Citation
APA
Chicago
ICMJE
MLA
NLM
Baldwin, S. W., & Aubé, J. (1987). Asymmetric synthesis with chiral hydroxylamines. Synthesis of optically pure 4-substituted azetidinones. Tetrahedron Letters, 28(2), 179–182. https://doi.org/10.1016/S0040-4039(00)95680-6
Baldwin, S. W., and J. Aubé. “Asymmetric synthesis with chiral hydroxylamines. Synthesis of optically pure 4-substituted azetidinones.” Tetrahedron Letters 28, no. 2 (January 1, 1987): 179–82. https://doi.org/10.1016/S0040-4039(00)95680-6.
Baldwin SW, Aubé J. Asymmetric synthesis with chiral hydroxylamines. Synthesis of optically pure 4-substituted azetidinones. Tetrahedron Letters. 1987 Jan 1;28(2):179–82.
Baldwin, S. W., and J. Aubé. “Asymmetric synthesis with chiral hydroxylamines. Synthesis of optically pure 4-substituted azetidinones.” Tetrahedron Letters, vol. 28, no. 2, Jan. 1987, pp. 179–82. Scopus, doi:10.1016/S0040-4039(00)95680-6.
Baldwin SW, Aubé J. Asymmetric synthesis with chiral hydroxylamines. Synthesis of optically pure 4-substituted azetidinones. Tetrahedron Letters. 1987 Jan 1;28(2):179–182.
Published In
Tetrahedron Letters
DOI
ISSN
0040-4039
Publication Date
January 1, 1987
Volume
28
Issue
2
Start / End Page
179 / 182
Related Subject Headings
- Organic Chemistry
- 0305 Organic Chemistry
- 0304 Medicinal and Biomolecular Chemistry