Stereoselective Synthesis of (±)-methyl Nonactate
Publication
, Journal Article
Baldwin, SW; Mclver, JM
Published in: Journal of Organic Chemistry
January 1, 1987
Racemic methyl nonactate has been prepared in 11 steps from 2,2-dimethyl-3(2H)-furanone with the diastereoisomeric relationships between C-2 and C-3, C-3 and C-6, and C-6 and C-8 established with stereoselectivities of 32:1, 50:1, and 24:1, respectively. © 1987, American Chemical Society. All rights reserved.
Duke Scholars
Published In
Journal of Organic Chemistry
DOI
EISSN
1520-6904
ISSN
0022-3263
Publication Date
January 1, 1987
Volume
52
Issue
2
Start / End Page
320 / 322
Related Subject Headings
- Organic Chemistry
- 3405 Organic chemistry
- 3404 Medicinal and biomolecular chemistry
- 0305 Organic Chemistry
- 0304 Medicinal and Biomolecular Chemistry
Citation
APA
Chicago
ICMJE
MLA
NLM
Baldwin, S. W., & Mclver, J. M. (1987). Stereoselective Synthesis of (±)-methyl Nonactate. Journal of Organic Chemistry, 52(2), 320–322. https://doi.org/10.1021/jo00378a043
Baldwin, S. W., and J. M. Mclver. “Stereoselective Synthesis of (±)-methyl Nonactate.” Journal of Organic Chemistry 52, no. 2 (January 1, 1987): 320–22. https://doi.org/10.1021/jo00378a043.
Baldwin SW, Mclver JM. Stereoselective Synthesis of (±)-methyl Nonactate. Journal of Organic Chemistry. 1987 Jan 1;52(2):320–2.
Baldwin, S. W., and J. M. Mclver. “Stereoselective Synthesis of (±)-methyl Nonactate.” Journal of Organic Chemistry, vol. 52, no. 2, Jan. 1987, pp. 320–22. Scopus, doi:10.1021/jo00378a043.
Baldwin SW, Mclver JM. Stereoselective Synthesis of (±)-methyl Nonactate. Journal of Organic Chemistry. 1987 Jan 1;52(2):320–322.
Published In
Journal of Organic Chemistry
DOI
EISSN
1520-6904
ISSN
0022-3263
Publication Date
January 1, 1987
Volume
52
Issue
2
Start / End Page
320 / 322
Related Subject Headings
- Organic Chemistry
- 3405 Organic chemistry
- 3404 Medicinal and biomolecular chemistry
- 0305 Organic Chemistry
- 0304 Medicinal and Biomolecular Chemistry