Synthetic study on chiral building block of vicinal diol, chiron approach to the precursors of all sphingosine stereoisomers

DOI: 10.1016/S0040-4020(01)89265-6

Source and publish data:

Tetrahedron p. 10727 - 10738 (1994)

Update date:2022-08-02

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Authors:

Li, Yun-Long

Sun, Xiao-Ling

Wu, Yu-Lin

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Article abstract of DOI:10.1016/S0040-4020(01)89265-6

All enantiomeric stereoisomers of 1,2,3-trihydroxy-4E-octadecene, key intermediates for the syntheses of sphingosines, were prepared using sugar as chiral pool.

Full text of DOI:10.1016/S0040-4020(01)89265-6

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Product name:4-Nitro-benzoic acid (E)-(S)-1-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-hexadec-2-enyl ester

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