SYNTHETIC STRATEGIES TO ACETOGENINS - THE HYDROXYBUTENOLIDE TERMINUS

被引：16

作者：

TROST, BM

CALKINS, TL

机构：

[1] Department of Chemistry Stanford University Stanford

来源：

TETRAHEDRON LETTERS | 1995年 / 36卷 / 34期

关键词：

D O I：

10.1016/0040-4039(95)01191-J

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Oxygen may be introduced to either carbon of 2-allylbutenolides, allowing a simple terminal alkene to be the structural precursor of the hydroxybutenolide tail of acetogenins via ruthenium and osmium catalyzed reactions.

引用

页码：6021 / 6024

页数：4

共 22 条

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[J]. TETRAHEDRON LETTERS, 1994, 35 (41) : 7517 - 7520
[6] TOTAL SYNTHESIS OF THE POTENT ANTITUMOR, BIS-TETRAHYDROFURANYL ANNONACEOUS ACETOGENINS (+)-ASIMICIN AND (+)-BULLATACIN
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[J]. TETRAHEDRON LETTERS, 1995, 36 (12) : 1981 - 1984
[7] STEREOSTRUCTURAL STUDIES ON THE 4-HYDROXYLATED ANNONACEOUS ACETOGENINS - A NOVEL USE OF MOSHER ESTER DATA FOR DETERMINING RELATIVE CONFIGURATION [BETWEEN C(4) AND C(36)]
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[J]. TETRAHEDRON LETTERS, 1994, 35 (46) : 8529 - 8532
[8] ORGANIC-SYNTHESIS WITH ENZYMES .3. TBADH-CATALYZED REDUCTION OF CHLORO KETONES - TOTAL SYNTHESIS OF (+)-(S,S)-(CIS-6-METHYLTETRAHYDROPYRAN-2-YL)ACETIC ACID - A CIVET CONSTITUENT
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