Synthesis of Spirocyclic Ethers

被引：58

作者：

Rosenberg, Sara ^{[1
]}

Leino, Reko ^{[1
]}

机构：

[1] Abo Akad Univ, Organ Chem Lab, SF-20500 Turku, Finland

来源：

SYNTHESIS-STUTTGART | 2009年 / 16期

基金：

芬兰科学院;

关键词：

spiro compounds; ethers; ring closure; stereoselective synthesis; natural products; RING-CLOSING METATHESIS; STEREOCONTROLLED TOTAL-SYNTHESIS; DIELS-ALDER REACTIONS; PHOSPHORUS-NITROGEN COMPOUNDS; PUMMERER REACTION CHEMISTRY; INTRAMOLECULAR S(N)2' OXASPIROCYCLIZATION; CYCLIZATION-CYCLOADDITION REACTION; SPIRO-FUSED 2,5-CYCLOHEXADIENONES; ENANTIOSELECTIVE TOTAL-SYNTHESIS; QUATERNARY CARBON STEREOCENTERS;

D O I：

10.1055/s-0029-1216892

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Spirocycles, including spirocyclic ethers, occur frequently in natural products and pharmaceutically active substances. Accordingly, synthetic methodologies utilized for the preparation of such compounds are of broad interest. The present review focuses on the general synthetic approaches that have been utilized for the construction of spirocyclic ethers during the past two decades.

引用

页码：2651 / 2673

页数：23

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