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. 2017 Jun 3;68(11):2951–2962. doi: 10.1093/jxb/erx156

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© The Author 2017. Published by Oxford University Press on behalf of the Society for Experimental Biology.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 2. — Structural elucidation of compounds in fractions 1, 2, and 3. (A) ¹H-NMR spectrum of compound in fraction 1 (CDCl₃, 400 MHz). (B) ¹H-NMR spectrum of compound in fraction 2 (CDCl₃, 400 MHz). (C) HRESIMS of compound in fraction 1 (ESI⁻). (D) HRESIMS of compound in fraction 2 (ESI⁻). (E) HRESIMS of compound in fraction 3 (ESI⁻). (F) Comparison of methyl derivatives of compounds in fractions 1, 2, and 3 with a standard fatty acid methyl ester mix.