A chiral LC–MS strategy for stereochemical assignment of natural products sharing a 3-methylpent-4-en-2-ol moiety in their terminal structures

Rei Suo, Raku Irie, Hinako Nakayama, Yuta Ishimaru, Yuya Akama, Masato Oikawa and Shiro Itoi
Beilstein J. Org. Chem. 2025, 21, 2243–2249. https://doi.org/10.3762/bjoc.21.171

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Supporting Information File 1: Experimental section, LC–MS chromatograms and NMR spectra.
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A chiral LC–MS strategy for stereochemical assignment of natural products sharing a 3-methylpent-4-en-2-ol moiety in their terminal structures
Rei Suo, Raku Irie, Hinako Nakayama, Yuta Ishimaru, Yuya Akama, Masato Oikawa and Shiro Itoi
Beilstein J. Org. Chem. 2025, 21, 2243–2249. https://doi.org/10.3762/bjoc.21.171

How to Cite

Suo, R.; Irie, R.; Nakayama, H.; Ishimaru, Y.; Akama, Y.; Oikawa, M.; Itoi, S. Beilstein J. Org. Chem. 2025, 21, 2243–2249. doi:10.3762/bjoc.21.171

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