Zuber, G and Goldsmith, MR and Hopkins, TD and Beratan, DN and 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.
ISSN 1523-7060
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Abstract
(Chemical Equation Presented) 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. © 2005 American Chemical Society.
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Details
Item Type: |
Article
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Status: |
Published |
Creators/Authors: |
Creators | Email | Pitt Username | ORCID ![](/images/orcid_id_24x24.png) |
---|
Zuber, G | | | | Goldsmith, MR | | | | Hopkins, TD | | | | Beratan, DN | | | | Wipf, P | pwipf@pitt.edu | PWIPF | |
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Date: |
10 November 2005 |
Date Type: |
Publication |
Journal or Publication Title: |
Organic Letters |
Volume: |
7 |
Number: |
23 |
Page Range: |
5269 - 5272 |
DOI or Unique Handle: |
10.1021/ol052154v |
Schools and Programs: |
Dietrich School of Arts and Sciences > Chemistry |
Refereed: |
Yes |
ISSN: |
1523-7060 |
MeSH Headings: |
Biological Agents--analysis; Biological Agents--chemistry; Circular Dichroism; Ethers, Cyclic--analysis; Ethers, Cyclic--chemistry; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Stereoisomerism |
PubMed ID: |
16268555 |
Date Deposited: |
30 Oct 2013 16:50 |
Last Modified: |
02 Feb 2019 15:56 |
URI: |
http://d-scholarship-dev.library.pitt.edu/id/eprint/19934 |
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