Iridium-catalysed asymmetric allylic substitutions

被引:415
作者
Helmchen, Guenter [1 ]
Dahnz, Axel [1 ]
Duebon, Pierre [1 ]
Schelwies, Mathias [1 ]
Weihofen, Robert [1 ]
机构
[1] Univ Heidelberg, Inst Organ Chem, D-69120 Heidelberg, Germany
关键词
D O I
10.1039/b614169b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ir-Catalysed allylic substitution is supplementing the traditional Pd-catalysed variant. With simple, easily available monosubstituted allylic acetates and carbonates as substrates, Ir catalysts generally favour chiral, branched products, while Pd catalysts typically give rise to linear, achiral products. With phosphorus amidites as ligands, regioselectivities > 10 : 1 and enantiomeric excess in the range 95-99 %ee are currently routinely achieved. A broad range of nucleophiles can be employed: for example stabilised carbanions, amines including their sulfonyl- and diacyl-derivatives, phenolates and alkoxides. A few applications, based on combinations of the allylic substitution and ring closing metathesis, indicate considerable potential of the method for the synthesis of biologically active compounds.
引用
收藏
页码:675 / 691
页数:17
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