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Synthesis of both 2,3-erythro- and 2,3-threo-isomers of aplidiasphingosine, a marine terpenoid

Agricultural and Biological Chemistry (1987) 51(1) 217-224
DOI: 10.1080/00021369.1987.10867967
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Abstract

Both 2,3-erythro- and 2,3-threo-isomers of aplidiasphingosine were synthesized. By examining their 13C NMR spectra, 2,3-threo- and 13, 4-erythro-relative configurations are proposed for aplidiasphingosine. © 1987 by the Agricultural Chemical Society of Japan.

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Umemura, T., Mori, K., & Mori, K. (1987). Synthesis of both 2,3-erythro- and 2,3-threo-isomers of aplidiasphingosine, a marine terpenoid. Agricultural and Biological Chemistry, 51(1), 217–224. https://doi.org/10.1080/00021369.1987.10867967

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