Synthesis of sphingosine relatives, X. Synthesis of (2 S ,3 R 4 E )‐1‐ O ‐(β‐ D ‐glucopyranosyl)‐ N ‐[30′‐(linoleoyloxy)triacontanoyl]‐4‐icosasphingenine, a new esterified cerebroside isolated from human and pig epidermis | Zendy

Mori Kenji | Zendy; Matsuda Hiroyuki | Zendy

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Synthesis of sphingosine relatives, X. Synthesis of (2 S ,3 R 4 E )‐1‐ O ‐(β‐ D ‐glucopyranosyl)‐ N ‐[30′‐(linoleoyloxy)triacontanoyl]‐4‐icosasphingenine, a new esterified cerebroside isolated from human and pig epidermis

Author(s) -

Mori Kenji,

Matsuda Hiroyuki

Publication year - 1991

Publication title -

liebigs annalen der chemie

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 0170-2041

DOI - 10.1002/jlac.199119910197

Subject(s) - chemistry , cerebroside , sphingosine , stereochemistry , linoleic acid , ceramide , biochemistry , fatty acid , apoptosis , receptor

(2 S ,3 R ,4 E )‐1‐ O ‐(β‐ D ‐Glucopyranosyl)‐ N ‐[30′‐(linoleoyloxy)triacontanoyl]‐4‐icosasphingenine ( 1 ) was synthesized from D ‐glucose, L ‐serine, 15‐pentadecanolide, and linoleic acid. The high‐field 1 H‐NMR spectrum of 1 was identical with that of the esterified cerebroside isolated from human and pig epidermis.

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