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Iridium-catalyzed cascade decarbonylation/highly enantioselective Pauson-Khand-type cyclization reactions

机译:铱催化的级联脱羰/高对映选择性的Pauson-Khand型环化反应

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摘要

An easily accessible chiral iridium-BINAP complex can effect the cooperative processes of decarbonylation of an aldehyde and cascaded enantioselective Pauson-Khand-type reaction. A survey of ligands revealed that atropisomeric aryl-diphosphine ligands were superior to chiral alkyl-diphosphines in this dual catalysis. Applying the reaction conditions of [IrCl(COD)](2)/(S)-BINAP complex with nonylaldehyde as a CO surrogate at 100 degrees C in anhydrous dioxane solvent, various 1,6-enynes were transformed to the corresponding optically active bicyclic cyclopentenones with excellent enantioselectivities (up to 98% ee). (c) 2006 Elsevier Ltd. All rights reserved.
机译:易于获得的手性铱-BINAP复合物可以实现醛脱羰和级联对映选择性Pauson-Khand型反应的协同过程。配体的调查显示,在这种双重催化中,阻转异构体的芳基-二膦配体优于手性烷基-二膦。在无水二恶烷溶剂中,以[IrCl(COD)](2)/(S)-BINAP配合物与壬基醛作为CO替代物的反应条件,在100°C的条件下,将各种1,6-烯炔转化为相应的旋光双环具有出色的对映选择性(高达98%ee)的环戊烯酮。 (c)2006 Elsevier Ltd.保留所有权利。

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