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  Assignment of the absolute configuration of aurantoside G and J.

Reinscheid, F., & Reinscheid, U. M. (2017). Assignment of the absolute configuration of aurantoside G and J. Journal of Molecular Structure, 1147, 96-102. doi:10.1016/j.molstruc.2017.05.139.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-002D-E4B8-F Version Permalink: https://hdl.handle.net/11858/00-001M-0000-002D-E4BB-9
Genre: Journal Article

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2478939.pdf (Publisher version), 622KB
 
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Reinscheid, F.1, Author           
Reinscheid, U. M.1, Author           
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1Department of NMR Based Structural Biology, MPI for Biophysical Chemistry, Max Planck Society, ou_578567              

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Free keywords: Aurantoside; Configuration; Optical rotation; DFT; Conformation
 Abstract: The analysis of C-13 and H-1 chemical shifts together with the specific optical rotation supports the claim that the natural product named aurantoside G has actually been synthesized recently. This result is based on the comparison of experimental and calculated data. Using the same procedure, evidences for the correct stereodescription of aurantoside J are also put forward. (C) 2017 Elsevier B.V. All rights reserved.

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Language(s): eng - English
 Dates: 2017-06-202017-11-05
 Publication Status: Issued
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 Rev. Type: Peer
 Identifiers: DOI: 10.1016/j.molstruc.2017.05.139
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Title: Journal of Molecular Structure
Source Genre: Journal
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Pages: - Volume / Issue: 1147 Sequence Number: - Start / End Page: 96 - 102 Identifier: -