TOTAL SYNTHESIS OF NOVEL GEOMETRIC ISOMERS OF LIPOXIN-A4 AND LIPOXIN-B4

被引：40

作者：

NICOLAOU, KC

MARRON, BE

VEALE, CA

WEBBER, SE

SERHAN, CN

机构：

[1] BRIGHAM & WOMENS HOSP,DIV HEMATOL,BOSTON,MA 02115

[2] HARVARD UNIV,SCH MED,BOSTON,MA 02115

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1989年 / 54卷 / 23期

关键词：

D O I：

10.1021/jo00284a026

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：5527 / 5535

页数：9

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[5]

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[6] STEREOSELECTIVE TOTAL SYNTHESIS OF THE PRESUMED BIOSYNTHETIC PRECURSOR TO LIPOXINS-A AND LIPOXINS-B - METHYL (7E,9E,11Z,13E,5S,6S,15S)-5,6-EPOXY-15-HYDROXYICOSA-7,9,11,13-TETRA-ENOATE AND ITS 5,6-METHANO ANALOG [J].

NICOLAOU, KC ;

WEBBER, SE .

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[7] STEREOCONTROLLED TOTAL SYNTHESIS OF LIPOXINS-A [J].

NICOLAOU, KC ;

VEALE, CA ;

WEBBER, SE ;

KATERINOPOULOS, H .

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[8]

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[9]

NICOLAOU KC, IN PRESS BIOCH BIOPH

[10]

NICOLAOU KC, 1986, SYNTHESIS-STUTTGART, V6, P453

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