AN UNUSUAL REARRANGEMENT OF A DIEPOXIDE

被引：4

作者：

CHAMBERS, RD

VAUGHAN, JFS

MULLINS, SJ

机构：

来源：

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS | 1995年 / 06期

关键词：

D O I：

10.1039/c39950000629

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The diepoxide derived from perfluoro-3,4-dimethyl-2,4-diene undergoes quantitative rearrangement, at 200 degrees C, to the corresponding 1,4-dioxine derivative.

引用

页码：629 / 629

页数：1

共 5 条

[1] A SYNTHESIS OF NOVEL PERFLUORODIENES [J].

BRISCOE, MW ;

CHAMBERS, RD ;

MULLINS, SJ ;

NAKAMURA, T ;

DRAKESMITH, FG .

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1990, (16) :1127-1128

[2] REACTIONS INVOLVING FLUORIDE-ION .38. NEW FLUORINATED DIENES BY DEFLUORINATION [J].

BRISCOE, MW ;

CHAMBERS, RD ;

MULLINS, SJ ;

NAKAMURA, T ;

VAUGHAN, JFS ;

DRAKESMITH, FG .

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1994, (21) :3115-3118

[3]

KOLENKO IP, 1979, IAN SSSR KH, V11, P2509

[4]

MERENYL R, 1986, SUBSTITUENT EFFECTS

[5] A STEREOCONTROLLED APPROACH TO ELECTROPHILIC EPOXIDES [J].

METHCOHN, O ;

MOORE, C ;

TALJAARD, HC .

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1988, (09) :2663-2674

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