Catalytic Asymmetric Alkylation of Aldehydes by Using Trialkylboranes

Triethylborane can be used in the asymmetric alkylation of aldehydes by using a 3‐(3,5‐diphenylphenyl)‐H8‐BINOL‐derived titanium(IV) catalyst in the presence of an excess amount of titanium tetraisopropoxide. The reaction proceeds with a low catalyst loading (2 mol‐%), exhibiting high enantioselecti...

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Veröffentlicht in:European Journal of Organic Chemistry 2008-09, Vol.2008 (26), p.4405-4407
Hauptverfasser: Ukon, Takahiro, Harada, Toshiro
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description Triethylborane can be used in the asymmetric alkylation of aldehydes by using a 3‐(3,5‐diphenylphenyl)‐H8‐BINOL‐derived titanium(IV) catalyst in the presence of an excess amount of titanium tetraisopropoxide. The reaction proceeds with a low catalyst loading (2 mol‐%), exhibiting high enantioselectivity for aromatic and unsaturated aldehydes. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008) Triethylborane can be used in the asymmetric alkylation of aldehydes by using a 3‐(3,5‐diphenylphenyl)‐H8‐BINOL‐derived titanium(IV) catalyst in the presence of an excess amount of titanium tetraisopropoxide.The reaction proceeds with a low catalyst loading (2 mol‐%), exhibiting high enantioselectivity for aromatic and unsaturated aldehydes.
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The reaction proceeds with a low catalyst loading (2 mol‐%), exhibiting high enantioselectivity for aromatic and unsaturated aldehydes. (© Wiley‐VCH Verlag GmbH &amp; Co. KGaA, 69451 Weinheim, Germany, 2008) Triethylborane can be used in the asymmetric alkylation of aldehydes by using a 3‐(3,5‐diphenylphenyl)‐H8‐BINOL‐derived titanium(IV) catalyst in the presence of an excess amount of titanium tetraisopropoxide.The reaction proceeds with a low catalyst loading (2 mol‐%), exhibiting high enantioselectivity for aromatic and unsaturated aldehydes.</description><identifier>ISSN: 1434-193X</identifier><identifier>EISSN: 1099-0690</identifier><identifier>DOI: 10.1002/ejoc.200800561</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>Alkylation ; Asymmetric catalysis ; asymmetric synthesis ; Boron ; Titanium</subject><ispartof>European Journal of Organic Chemistry, 2008-09, Vol.2008 (26), p.4405-4407</ispartof><rights>Copyright © 2008 WILEY‐VCH Verlag GmbH &amp; Co. 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KGaA, 69451 Weinheim, Germany, 2008) Triethylborane can be used in the asymmetric alkylation of aldehydes by using a 3‐(3,5‐diphenylphenyl)‐H8‐BINOL‐derived titanium(IV) catalyst in the presence of an excess amount of titanium tetraisopropoxide.The reaction proceeds with a low catalyst loading (2 mol‐%), exhibiting high enantioselectivity for aromatic and unsaturated aldehydes.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/ejoc.200800561</doi><tpages>3</tpages></addata></record>
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source Wiley Online Library Journals Frontfile Complete
subjects Alkylation
Asymmetric catalysis
asymmetric synthesis
Boron
Titanium
title Catalytic Asymmetric Alkylation of Aldehydes by Using Trialkylboranes
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