Published March 31, 2023 | Version v1
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Fig. 1 in On the configuration and occurrence of 2,6-cyclocuparan-3-ols: Resolving a lasting discrepancy

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Fig. 1. Structures of diastereomeric cyclocuparanols as reported in the literature. The carbon numbering scheme is taken from Dictionary of Natural Products (Dictionary of Natural Products on CD-ROM et al., 1999).

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Published as part of Zlatkovi, Dragan B., c, Đorđevic, Miljana R., Zlatkovi, c & Radulovic, Niko S., 2023, On the configuration and occurrence of 2,6-cyclocuparan-3-ols: Resolving a lasting discrepancy, pp. 1-10 in Phytochemistry (113566) 207 on page 2, DOI: 10.1016/j.phytochem.2022.113566, http://zenodo.org/record/8290501

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Journal article: 10.1016/j.phytochem.2022.113566 (DOI)
Journal article: urn:lsid:plazi.org:pub:CB4BFF9DFFB3F953367B7533512FFFBF (LSID)
Journal article: https://zenodo.org/record/8290501 (URL)