BENZOTHIADIPHOSPHOLE AS PHOSPHORUS DONATING REAGENT FOR A NEW ROUTE TO 2H-1,2,3-DIAZAPHOSPHOLE DERIVATIVES

被引：22

作者：

BACCOLINI, G

ORSOLAN, G

MEZZINA, E

机构：

[1] Dipartimento di Chimica Organica, Università, 40136 Bologna

来源：

TETRAHEDRON LETTERS | 1995年 / 36卷 / 03期

关键词：

D O I：

10.1016/0040-4039(94)02281-F

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Conjugated azoalkenes 2 react at reflux toluene with fused benzothiadiphosphole 1 (or 4) to give the diazaphosphole 3 in 25-52% yields. With this route it is possible to isolate the so far unknown 3a which is difficult to obtain in other reported conditions. The P atom involved in this cycloaddition is the one between the two S atoms.

引用

页码：447 / 450

页数：4

共 26 条

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