Hydroxy group directivity in the epoxidation of chiral allylic alcohols: Control of diastereoselectivity through allylic strain and hydrogen bonding

被引：155

作者：

Adam, W ^{[1
]}

Wirth, T ^{[1
]}

机构：

[1] Univ Wurzburg, Inst Organ Chem, D-97074 Wurzburg, Germany

来源：

ACCOUNTS OF CHEMICAL RESEARCH | 1999年 / 32卷 / 08期

关键词：

D O I：

10.1021/ar9800845

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

[No abstract available]

引用

收藏

页码：703 / 710

页数：8

相关论文

共 43 条

[41] Heterogeneous catalysts for liquid-phase oxidations: Philosophers' stones or Trojan horses?
Sheldon, RA
Wallau, M
Arends, IWCE
Schuchardt, U
[J]. ACCOUNTS OF CHEMICAL RESEARCH, 1998, 31 (08) : 485 - 493
[42] Experimental geometry of the epoxidation transition state
Singleton, DA
Merrigan, SR
Liu, J
Houk, KN
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (14) : 3385 - 3386
[43] THE ROLE OF TRIMETHYLSILYL GROUP IN HIGHLY STEREOSELECTIVE EPOXIDATION OF ALLYLIC ALCOHOLS
TOMIOKA, H
SUZUKI, T
OSHIMA, K
NOZAKI, H
[J]. TETRAHEDRON LETTERS, 1982, 23 (33) : 3387 - 3390

← 1 2 3 4 5 →