RECENT ADVANCES IN SYNTHETIC METHOD OF NITROGEN-HETEROCYCLES VIA AZA-WITTIG REACTION

被引：12

作者：

EGUCHI, S

OKANO, T

机构：

[1] Institute of Applied Organic Chemistry, Department of Applied Chemistry, Faculty of Engineering, Nagoya University

来源：

JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN | 1993年 / 51卷 / 03期

关键词：

IMINOPHOSPHORANE; LAMBDA(5)-PHOSPHAZENE; AZIDE; PHOSPHOROUS(III) COMPOUNDS; STAUDINGER REACTION; AZA-WITTIG REACTION; TANDEM STAUDINGER REACTION AZA-WITTIG REACTION; TANDEM AZA-WITTIG REACTION ELECTROCYCLIC REACTION; PHOSPHAZIDE; NITROGEN HETEROCYCLES;

D O I：

10.5059/yukigoseikyokaishi.51.203

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Recent advances in synthetic method of heterocyclic compounds by aza-Wittig reaction, i.e. , the imination using iminophosphoranes, are here reviewed. Examples are systematically presented depending on the direct cyclization route by intramolecular aza-Wittig reaction, or the sequential route via intermolecular aza-Wittig reaction, followed by various types of cyclizations such as electrocyclic reaction, Diels-Alder cycloaddition, and nucleophilic heterocyclization etc. The feasibility of this method in synthesis of nitrogen-heterocycles is emphasized in this review.

引用

页码：203 / 211

页数：9

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