Further observations on the rhodium (I)-catalysed tandem hydrosilylation-intramolecular aldol reaction

被引：43
作者：
Freiría, M
Whitehead, AJ
Tocher, DA
Motherwell, WB
机构：
[1] UCL, Dept Chem, Christopher Ingold Labs, London WC1H 0AJ, England
[2] GlaxoSmithKline Res & Dev Ltd, Chem Dev Div, Stevenage SG1 2NY, Herts, England
来源：
TETRAHEDRON | 2004年 / 60卷 / 11期
关键词：
tandem hydrosilylation; aldol; rhodium; intramolecular; catalytic;
D O I：
10.1016/j.tet.2003.12.057
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
The rhodium (1) catalysed tandem hydrosilylation-intramolecular aldol reaction provides a simple strategy for construction of a range of usefully functionalised five-membered rings from readily prepared 6-oxo-2-hexenoates in good yield and with good to excellent stereoselectivity. A series of silanes and rhodium catalysts have been investigated. Stereoselectivity proved to be highly dependant on the catalyst as well as on the substitution pattern of the parent substrate. The extension of this methodology for the synthesis of larger ring sizes has also been evaluated. (C) 2004 Elsevier Ltd. All rights reserved.
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收藏
页码：2673 / 2692
页数：20
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