Lewis base catalyzed asymmetric reactions involving hypervalent silicate intermediates
被引:123
作者:
Orito, Y
论文数: 0引用数: 0
h-index: 0
机构:
Kumamoto Univ, Fac Med & Pharmaceut Sci, Kumamoto 8620973, JapanKumamoto Univ, Fac Med & Pharmaceut Sci, Kumamoto 8620973, Japan
Orito, Y
[1
]
Nakajima, M
论文数: 0引用数: 0
h-index: 0
机构:
Kumamoto Univ, Fac Med & Pharmaceut Sci, Kumamoto 8620973, JapanKumamoto Univ, Fac Med & Pharmaceut Sci, Kumamoto 8620973, Japan
Nakajima, M
[1
]
机构:
[1] Kumamoto Univ, Fac Med & Pharmaceut Sci, Kumamoto 8620973, Japan
来源:
SYNTHESIS-STUTTGART
|
2006年
/
09期
关键词:
asymmetric;
organocatalysis;
hypervalent silicon;
Lewis base;
stereoselectivity;
D O I:
10.1055/s-2006-926405
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
The development of catalytic enantioselective reactions is a challenging area in synthetic organic chemistry. In the last decade, numerous chiral metal complexes, which act as Lewis acids, have been very successful. However, Lewis base catalyzed asymmetric reactions are also attracting attention. Recent developments in silicon-based chemistry have led to new asymmetric reactions, which involve so-called hypervalent silicates as intermediates, wherein new types of organocatalysts are often utilized as promoters. This review presents the progress in silicate-mediated asymmetric reactions catalyzed by chiral Lewis bases, particularly those based on various types of silicon Compounds.