CHIRAL EPOXIDES FOR LEUKOTRIENE SYNTHESES - A D-XYLOSE APPROACH

被引：7

作者：

POUGNY, JR ^{[1
]}

ROLLIN, P ^{[1
]}

机构：

[1] UFR FAC SCI ORLEANS,BIOCHIM STRUCT LAB,UNITE 499,BP 6759,F-45067 ORLEANS 2,FRANCE

来源：

JOURNAL OF CARBOHYDRATE CHEMISTRY | 1986年 / 5卷 / 04期

关键词：

D O I：

10.1080/07328308608062985

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：701 / 704

页数：4

共 17 条

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GOTO, G .

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[3] STEREOSPECIFIC TOTAL SYNTHESIS OF A SLOW REACTING SUBSTANCE OF ANAPHYLAXIS, LEUKOTRIENE C-1 [J].

COREY, EJ ;

CLARK, DA ;

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MARFAT, A ;

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SAMUELSSON, B ;

HAMMARSTROM, S .

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[4] CHEMICAL STUDIES ON SLOW REACTING SUBSTANCES LEUKOTRIENES [J].

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[5] A SIMPLE METHOD FOR TOSYLATION WITH INVERSION [J].

GALYNKER, I ;

STILL, WC .

TETRAHEDRON LETTERS, 1982, 23 (43) :4461-4464

[6]

MORIN C, 1983, J CHEM RES, P2524

[7] LEUKOTRIENE-C - SLOW-REACTING SUBSTANCE FROM MURINE MASTOCYTOMA-CELLS [J].

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HAMMARSTROM, S ;

SAMUELSSON, B .

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[8]

ORMING L, 1980, P NATL ACAD SCI, V77, P2014

[9]

PIANETTI P, IN PRESS TETRAHEDRON

[10] THE STEREOSPECIFIC SYNTHESIS OF LEUKOTRIENE-A4 (LTA4), 5-EPI-LTA4, 6-EPI-LTA4 AND 5-EPI,6-EPI-LTA4 [J].

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ZAMBONI, R ;

LAU, CK ;

GUINDON, Y .

TETRAHEDRON LETTERS, 1981, 22 (29) :2759-2762

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