SYNTHESIS OF 1,3-DIKETONES USING ALPHA-DIAZO KETONES AND ALDEHYDES IN THE PRESENCE OF TIN(II) CHLORIDE

被引：77

作者：

PADWA, A

HORNBUCKLE, SF

ZHANG, Z

ZHI, L

机构：

[1] Department of Chemistry, Emory University, Atlanta

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1990年 / 55卷 / 18期

关键词：

D O I：

10.1021/jo00305a029

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Recent publications from our laboratory have introduced a new general strategy for oxapolycyclic ring synthesis in which a rhodium(II)-catalyzed tandem cyclization-cyclo-addition reaction represents the central element.1 For ongoing studies to further implement and develop this strategy, we required a general route to a-diazo 1,3-di-ketones, which serve as the precursors for carbonyl ylide dipoles of type 2. Highly stabilized β-dicarbonyl enolates. © 1990, American Chemical Society. All rights reserved.

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页码：5297 / 5299

页数：3

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