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Synthesis of racemic erythro-dihydrosphingosine

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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

Racemic erythro-dihydrosphingosine was synthesized by hydroxymethylation and cleavage of 4-palmityl-5-oxazolinone with subsequent reduction and saponification of the intermediate 1-hydroxy-2-benzamido-3-octadecanone.

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Literature cited

  1. S. I. Zav'yalov, N. I. Aronova, N. N. Makhova, V. I. Gunar, L. F. Ovechkina, N. A. Rodionova, and E. P. Gracheva, Izv. Akad. Nauk SSSR, Ser. Khim., 1119 (1970).

  2. N. I. Aronova, N. N. Makhova, and S. I. Zav'yalov, Izv. Akad. Nauk SSSR, Ser. Khim., 724 (1970).

  3. W. Stoffel, D. Lekim, and G. Sticht, Z. Phys. Chem.,349, 664 (1968).

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Authors and Affiliations

  1. N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the USSR, USSR

    S. I. Zav'yalov, N. N. Makhova & N. I. Aronova

Authors
  1. S. I. Zav'yalov
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  2. N. N. Makhova
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  3. N. I. Aronova
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 6, pp. 1445–1446, June, 1972.

We sincerely thank R. P. Evstigneeva and E. N. Zvonkova for furnishing us with a sample of VII.

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Zav'yalov, S.I., Makhova, N.N. & Aronova, N.I. Synthesis of racemic erythro-dihydrosphingosine. Russ Chem Bull 21, 1401–1402 (1972). https://doi.org/10.1007/BF00854580

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  • DOI: https://doi.org/10.1007/BF00854580

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