Anti-selective epoxidation of primary 5-(tert-butyl-dimethylsilyl)oxyallylic alcohols with m-chloroperoxybenzoic acid

被引：0

作者：

Jorgensen, KB ^{[1
]}

Koshino, H ^{[1
]}

Nakata, T ^{[1
]}

机构：

[1] RIKEN, Inst Phys & Chem Res, Wako, Saitama 35101, Japan

来源：

HETEROCYCLES | 1998年 / 47卷 / 02期

关键词：

D O I：

暂无

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Epoxidation of primary 5-(tert-butyldimethylsilyl)oxyallylic alcohols with m-chloroperoxybenzoic acid produced anti-epoxides with high stereoselectivity.

引用

页码：679 / 683

页数：5

共 3 条

[1] Experimental investigation of the primary and secondary deuterium kinetic isotope effects for epoxidation of alkenes and ethylene with m-chloroperoxybenzoic acid
Koerner, T
Slebocka-Tilk, H
Brown, RS
[J]. JOURNAL OF ORGANIC CHEMISTRY, 1999, 64 (01): : 196 - 201
[2] Experimental investigation of the primary and secondary deuterium kinetic isotope effects for epoxidation of alkenes and ethylene with m-chloroperoxybenzoic acid
[J]. J Org Chem, 1 (196-201):
[3] Highly stereoselective epoxidation of a 4-methyl-5-(triethylsilyl)oxyallyl alcohol system with m-chloroperoxybenzoic acid
Maruyama, K
Ueda, M
Sasaki, S
Iwata, Y
Miyazawa, M
Miyashita, M
[J]. TETRAHEDRON LETTERS, 1998, 39 (25) : 4517 - 4520

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