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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.
Journal cover image

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