AN EFFICIENT SYNTHESIS OF LEUKOTRIENE-B4

被引：17

作者：

AVIGNONTROPIS, M ^{[1
]}

TREILHOU, M ^{[1
]}

LEBRETON, J ^{[1
]}

POUGNY, JR ^{[1
]}

FRECHARDORTUNO, I ^{[1
]}

HUYNH, C ^{[1
]}

LINSTRUMELLE, G ^{[1
]}

机构：

[1] ECOLE NORM SUPER,CNRS,CHIM LAB,F-75231 PARIS 05,FRANCE

来源：

TETRAHEDRON LETTERS | 1989年 / 30卷 / 46期

关键词：

D O I：

10.1016/S0040-4039(01)93886-9

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：6335 / 6336

页数：2

共 8 条

[1]

AVIGNONTROPIS M, 1989, IN PRESS TETRAHEDRON, V30

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[3] HIGHLY STEREOCONTROLLED, MULTIGRAM SCALE SYNTHESIS OF LEUKOTRIENE-B4 [J].

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SHIMAZAKI, T ;

SATO, F .

TETRAHEDRON LETTERS, 1987, 28 (47) :5849-5852

[4] TOTAL SYNTHESIS OF LEUKOTRIENE-B4 [(+)-LTB4] AND HOMO-LTB4 FROM D-MANNITOL [J].

LEMERRER, Y ;

GRAVIERPELLETIER, C ;

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DUREAULT, A ;

DEPEZAY, JC .

JOURNAL OF ORGANIC CHEMISTRY, 1989, 54 (10) :2409-2416

[5] STEREOCONTROLLED TOTAL SYNTHESIS OF (5S,6R)-(7E,9E,11Z,14Z)-5-6-DIHYDROXY-7,9,11,14-ICOSATETRAENOIC, (5S,6S)-(7E,9E,11Z,14Z)-5-6-DIHYDROXY-7,9,11,14-ICOSATETRAENOIC, (5R,6R)-(7E,9E,11Z,14Z)-5-6-DIHYDROXY-7,9,11,14-ICOSATETRAENOIC, AND (5R,6S)-(7E,9E,11Z,14Z)-5,6-DIHYDROXY-7,9,11,14-ICOSATETRAENOIC ACID (5,6-DIHETE) METHYL-ESTERS [J].

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SPANEVELLO, RA .

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1989, 28 (05) :587-588

[6] A GENERAL AND STEREOCONTROLLED TOTAL SYNTHESIS OF LEUKOTRIENE-B4 AND ANALOGS [J].

NICOLAOU, KC ;

ZIPKIN, RE ;

DOLLE, RE ;

HARRIS, BD .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1984, 106 (12) :3548-3551

[7] OPTICALLY-ACTIVE PROPARGYLIC ALCOHOLS FROM D-XYLOSE USEFUL PRECURSORS FOR LTB4 SYNTHESIS [J].

PIANETTI, P ;

ROLLIN, P ;

POUGNY, JR .

TETRAHEDRON LETTERS, 1986, 27 (48) :5853-5856

[8] DRAMATIC RATE ENHANCEMENT OF SUZUKI DIENE SYNTHESIS - ITS APPLICATION TO PALYTOXIN SYNTHESIS [J].

UENISHI, J ;

BEAU, JM ;

ARMSTRONG, RW ;

KISHI, Y .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1987, 109 (15) :4756-4758

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