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Issue 24, 2016
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Towards theory driven structure elucidation of complex natural products: mandelalides and coibamide A

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Abstract

The effectiveness of computational tools in determining relative configurations of complex molecules is investigated, using natural products mandelalides A–D and coibamide A, towards a generalized recipe for the scientific community at large. Ultimately, continuing efforts in this vein will accelerate and strengthen relative structure elucidation of complex molecules, such as natural products. Molecular mechanics conformational search, quantum mechanical NMR chemical shift predictions, and DP4 analyses led to confirmation of the revised structures of mandelalides A–D and coibamide A. All chiral centers in the northern hemisphere of mandelalides A–D are inverted with respect to the originally proposed structures, in agreement with recent total syntheses of mandelalide A by Ye, Fürstner & Carter. In the case of coibamide A, it was found that Fang & Su's revision, in which both the macrocycle [MeAla11] and the side chain [HIV2] residues are inverted from L to D, was consistent with the authentic natural product and computations.

Graphical abstract: Towards theory driven structure elucidation of complex natural products: mandelalides and coibamide A

  • This article is part of the themed collection: New Talent
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Publication details

The article was received on 04 Apr 2016, accepted on 22 Apr 2016 and first published on 06 May 2016


Article type: Paper
DOI: 10.1039/C6OB00707D
Citation: Org. Biomol. Chem., 2016,14, 5826-5831
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    Towards theory driven structure elucidation of complex natural products: mandelalides and coibamide A

    K. M. Snyder, J. Sikorska, T. Ye, L. Fang, W. Su, R. G. Carter, K. L. McPhail and P. H.-Y. Cheong, Org. Biomol. Chem., 2016, 14, 5826
    DOI: 10.1039/C6OB00707D

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