Synthesis of sphingosine relatives. Part V Synthesis of both 2,3-erythro-and 2,3-threo-isomers of aplidiasphingosine, a marine terpenoid.
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- UMEMURA Takeaki
- Department of Agricultural Chemistry, The University of Tokyo on leave from Sumitomo Chemical Co.
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- MORI Kenji
- Department of Agricultural Chemistry, The University of Tokyo
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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, 14-erythro-relative configurations are proposed for aplidiasphingosine.
Journal
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- Agricultural and Biological Chemistry
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Agricultural and Biological Chemistry 51 (1), 217-224, 1987
Japan Society for Bioscience, Biotechnology, and Agrochemistry
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Keywords
Details 詳細情報について
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- CRID
- 1390282681444726272
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- NII Article ID
- 110006323125
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- NII Book ID
- AA00515312
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- COI
- 1:CAS:528:DyaL2sXmtlOjtLs%3D
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- ISSN
- 18811280
- 00021369
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- Text Lang
- en
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- Data Source
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- JaLC
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed