OXIDATIVE 1,2-ARYL REARRANGEMENT IN FLAVANONES USING THALLIUM(III) PARA-TOLYL SULFONATE (TTS) - A NEW USEFUL ROUTE TO ISOFLAVONES

被引：36

作者：

SINGH, OV ^{[1
]}

GARG, CP ^{[1
]}

KAPOOR, RP ^{[1
]}

机构：

[1] KURUKSHETRA UNIV, DEPT CHEM, KURUKSHETRA 132119, HARYANA, INDIA

来源：

TETRAHEDRON LETTERS | 1990年 / 31卷 / 19期

关键词：

D O I：

10.1016/S0040-4039(00)94689-6

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Oxidation of flavanones using thallium(III) p-tolylsulphonate (prepared in situ by the reaction of thallium(III) acetate and p-toluene sulphonic acid) in propionitrile leads to 1,2-aryl shift providing a new useful route to the synthesis of isoflavones. © 1990.

引用

页码：2747 / 2750

页数：4

共 19 条

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