RESEARCHES ON ACETYLENIC COMPOUNDS .21. REFORMATSKY REACTIONS WITH PROPARGYL BROMIDES

被引：76

作者：

HENBEST, HB

JONES, ERH

WALLS, IMS

机构：

来源：

JOURNAL OF THE CHEMICAL SOCIETY | 1949年 / OCT期

关键词：

D O I：

10.1039/jr9490002696

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：2696 / 2700

页数：5

共 8 条

[1] BABAYAN, 1939, CHEM ABSTR 9283, V33
[2] BABAYAN, 1938, CHEM ABSTR 7894, V32
[3] An acetylenic analog of neopentyl bromide, evidence that the hindrance to displacement reactions in neopentyl halides is steric in nature
Bartlett, PD
Rosen, LJ
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1942, 64 : 543 - 546
[4] JAPP, 1901, J CHEM SOC, P1019
[5] NIEUWLAND, 1931, J AM CHEM SOC, V53, P1842
[6] WISLICENUS, 1898, ANNALEN, V302, P216
[7] Some conversions of propargyl derivatives.
Zeile, K
Meyer, H
[J]. BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT, 1942, 75 : 356 - 362
[8] 1934, Z PHYSL CHEM, V225, P215