A CONVENIENT STEREOSELECTIVE SYNTHESIS OF D-ERYTHRO-C-18-SPHINGOSINE FROM GALACTAL

被引：40

作者：

HIRATA, N ^{[1
]}

YAMAGIWA, Y ^{[1
]}

KAMIKAWA, T ^{[1
]}

机构：

[1] KINKI UNIV,FAC SCI & TECHNOL,DEPT CHEM,OSAKA,OSAKA 577,JAPAN

来源：

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1991年 / 09期

关键词：

D O I：

10.1039/p19910002279

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The highly efficient stereoselective synthesis of D-erythro-C18-sphingosine from 3,4,6-tribenzyl-oxygalactal via 4,6-tribenzyloxy-5-hydroxyhexenal is described.

引用

页码：2279 / 2280

页数：2

共 7 条

[1]

DONDONI A, 1990, J ORG CHEM, V55, P1437

[2] A STEREODIVERGENT SYNTHESIS OF D-ERYTHRO-SPHINGOSINE AND D-THREO-SPHINGOSINE FROM L-SERINE [J].

GARNER, P ;

PARK, JM ;

MALECKI, E .

JOURNAL OF ORGANIC CHEMISTRY, 1988, 53 (18) :4395-4398

[3]

HAKOMORI S, 1983, HDB LIPID RES, V3, P1

[4]

OHASHI K, 1989, TETRAHEDRON, V45, P2257

[5] GQ1B, A BIOACTIVE GANGLIOSIDE THAT EXHIBITS NOVEL NERVE GROWTH-FACTOR (NGF)-LIKE ACTIVITIES IN THE 2 NEURO-BLASTOMA CELL-LINES [J].

TSUJI, S ;

ARITA, M ;

NAGAI, Y .

JOURNAL OF BIOCHEMISTRY, 1983, 94 (01) :303-306

[6]

WENGEL J, 1989, SYNTHESIS-STUTTGART, P829

[7]

1991, 61ST ANN M JAP CHEM, V2, P1686

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