FORMATION OF 14-MEMBERED CARBOCYCLES BY INTRAMOLECULAR MICHAEL ADDITION ON YNONES AND ENONES

被引：11

作者：

GIRARD, S ^{[1
]}

DESLONGCHAMPS, P ^{[1
]}

机构：

[1] UNIV SHERBROOKE,FAC SCI,DEPT CHIM,SYNTHESE ORGAN LAB,SHERBROOKE J1K 2R1,QUEBEC,CANADA

来源：

CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE | 1992年 / 70卷 / 05期

关键词：

D O I：

10.1139/v92-163

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The base-catalyzed intramolecular Michael addition of substituted malonates on ynones or enones proceeds efficiently to give the 14-membered carbocycles.

引用

页码：1265 / 1273

页数：9

共 8 条

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[2] SYNTHESIS OF 9-MEMBERED AND 10-MEMBERED RINGS BY THE INTRAMOLECULAR MICHAEL ADDITION OF MALONATE ON ENONE AND YNONE
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[5] INTRAMOLECULAR MICHAEL ADDITION OF CYCLIC BETA-KETOESTER ON CONJUGATED ACETYLENIC KETONE
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[J]. TETRAHEDRON LETTERS, 1986, 27 (45) : 5455 - 5458
[6] LAVALLEE JF, 1988, THESIS U SHERBROOKE
[7] OXIDATION OF LONG-CHAIN AND RELATED ALCOHOLS TO CARBONYLS BY DIMETHYL-SULFOXIDE ACTIVATED BY OXALYL CHLORIDE
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