Systematic assignment of the configuration of flexible natural products by spectroscopic and computational methods: the bistramide C analysis.
Publication
, Journal Article
Zuber, G; Goldsmith, M-R; Hopkins, TD; Beratan, DN; Wipf, P
Published in: Organic letters
November 2005
[reaction: see text] The combination of NMR NOE, chemical shift, and J-coupling measurements with molar rotation and circular dichroism (CD) determinations, including RI-DFT BP86/aug-cc-pVDZ calculations, reduced a candidate pool of 1024 possible stereoisomers of (+)-bistramide C to a single absolute configuration assignment for the 10 stereogenic carbons of the marine natural product.
Duke Scholars
Published In
Organic letters
DOI
EISSN
1523-7052
ISSN
1523-7060
Publication Date
November 2005
Volume
7
Issue
23
Start / End Page
5269 / 5272
Related Subject Headings
- Stereoisomerism
- Organic Chemistry
- Nuclear Magnetic Resonance, Biomolecular
- Molecular Structure
- Ethers, Cyclic
- Circular Dichroism
- Biological Products
- 03 Chemical Sciences
Citation
APA
Chicago
ICMJE
MLA
NLM
Zuber, G., Goldsmith, M.-R., Hopkins, T. D., Beratan, D. N., & Wipf, P. (2005). Systematic assignment of the configuration of flexible natural products by spectroscopic and computational methods: the bistramide C analysis. Organic Letters, 7(23), 5269–5272. https://doi.org/10.1021/ol052154v
Zuber, Gérard, Michael-Rock Goldsmith, Tamara D. Hopkins, David N. Beratan, and Peter Wipf. “Systematic assignment of the configuration of flexible natural products by spectroscopic and computational methods: the bistramide C analysis.” Organic Letters 7, no. 23 (November 2005): 5269–72. https://doi.org/10.1021/ol052154v.
Zuber G, Goldsmith M-R, Hopkins TD, Beratan DN, Wipf P. Systematic assignment of the configuration of flexible natural products by spectroscopic and computational methods: the bistramide C analysis. Organic letters. 2005 Nov;7(23):5269–72.
Zuber, Gérard, et al. “Systematic assignment of the configuration of flexible natural products by spectroscopic and computational methods: the bistramide C analysis.” Organic Letters, vol. 7, no. 23, Nov. 2005, pp. 5269–72. Epmc, doi:10.1021/ol052154v.
Zuber G, Goldsmith M-R, Hopkins TD, Beratan DN, Wipf P. Systematic assignment of the configuration of flexible natural products by spectroscopic and computational methods: the bistramide C analysis. Organic letters. 2005 Nov;7(23):5269–5272.
Published In
Organic letters
DOI
EISSN
1523-7052
ISSN
1523-7060
Publication Date
November 2005
Volume
7
Issue
23
Start / End Page
5269 / 5272
Related Subject Headings
- Stereoisomerism
- Organic Chemistry
- Nuclear Magnetic Resonance, Biomolecular
- Molecular Structure
- Ethers, Cyclic
- Circular Dichroism
- Biological Products
- 03 Chemical Sciences