ALPHA'-FUNCTIONALIZATION OF BETA,GAMMA-UNSATURATED CYCLOHEXENONES - UTILIZATION OF SILYL ENOL ETHERS PRODUCED FROM LITHIUM-AMMONIA - REDUCTION OF SILYL ARYL ETHERS

被引：23

作者：

DONALDSON, RE ^{[1
]}

FUCHS, PL ^{[1
]}

机构：

[1] PURDUE UNIV,DEPT CHEM,W LAFAYETTE,IN 47907

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1977年 / 42卷 / 11期

关键词：

D O I：

10.1021/jo00431a055

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：2032 / 2034

页数：3

共 24 条

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[3] REACTIONS OF SILYL ENOL ETHERS AND LACTONE ENOLATES WITH DIMETHYL(METHYLENE)AMMONIUM IODIDE - BIS-ALPHA-METHYLENATION OF PRE-VERNOLEPIN AND PRE-VERNOMENIN
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[4] STRAIN EFFECTS .I. HYDROXYMETHYLENE KETONE-ALDO ENOL EQUILIBRIUM
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[5] CHEMISTRY OF CARBANIONS .18. PREPARATION OF TRIMETHYLSILYL ENOL ETHERS
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[8] STEROID TOTAL SYNTHESIS - HYDROCHRYSENE APPROACH .7. METAL-IN-AMMONIA REDUCTION OF THE AROMATIC NUCLEUS - DL-EPIANDROSTERONE AND THE LUMI EPIMER
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[9] JUNG ME, 1976, TETRAHEDRON LETT, P2935
[10] QUATERNARY AMMONIUM ENOLATES AS SYNTHETIC INTERMEDIATES - REGIOSPECIFIC ALKYLATION REACTION OF KETONES
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