Asymmetric methoxyselenenylations with camphor-based selenium electrophiles

被引:29
作者
Back, TG [1 ]
Nan, S [1 ]
机构
[1] Univ Calgary, Dept Chem, Calgary, AB T2N 1N4, Canada
来源
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1998年 / 19期
关键词
D O I
10.1039/a806707d
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The asymmetric methoxyselenenylation of olefins was achieved with a series of camphor-based selenenyl triflates, of which the readily available 2-oxo analog 2a proved the most effective.
引用
收藏
页码:3123 / 3124
页数:2
相关论文
共 23 条
[11]  
FUJITA K, 1995, TETRAHEDRON LETT, V36, P5219
[12]   Design of optically active selenium reagents having a chiral tertiary amino group and their application to asymmetric inter- and intramolecular oxyselenenylations [J].
Fujita, K ;
Murata, K ;
Iwaoka, M ;
Tomoda, S .
TETRAHEDRON, 1997, 53 (06) :2029-2048
[13]   A HIGHLY SELECTIVE ASYMMETRIC METHOXYSELENYLATION OF ALKENES WITH A CHIRAL FERROCENYLSELENIUM REAGENT [J].
FUKUZAWA, S ;
KASUGAHARA, Y ;
UEMURA, S .
TETRAHEDRON LETTERS, 1994, 35 (50) :9403-9406
[14]   Asymmetric methoxyselenenylation of alkenes with chiral ferrocenylselenium reagents [J].
Fukuzawa, S ;
Takahashi, K ;
Kato, H ;
Yamazaki, H .
JOURNAL OF ORGANIC CHEMISTRY, 1997, 62 (22) :7711-7716
[15]  
NAN S, 1998, 80 ANN C CAN SOC CHE
[16]  
PAULMIER C, 1986, SELENIUM REAGENTS IN, pCH7
[17]  
Schmid G. H., 1977, CHEM DOUBLE BONDED F
[18]   Asymmetric selenomethoxylation of alkenes with camphorselenenyl sulfate [J].
Tiecco, M ;
Testaferri, L ;
Santi, C ;
Marini, F ;
Bagnoli, L ;
Temperini, A .
TETRAHEDRON LETTERS, 1998, 39 (18) :2809-2812
[19]   DOUBLE DIFFERENTIATION IN ASYMMETRIC METHOXYSELENENYLATION OF TRANS-BETA-METHYLSTYRENE [J].
TOMODA, S ;
FUJITA, K ;
IWAOKA, M .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1990, (02) :129-131
[20]   ASYMMETRIC TRANS-ADDITION REACTIONS OF A CHIRAL SELENOBINAPHTHYL WITH PROCHIRAL OLEFINS - THE CASE OF METHOXYSELENENYLATION [J].
TOMODA, S ;
IWAOKA, M .
CHEMISTRY LETTERS, 1988, (11) :1895-1898