A comparison of the Still-Gennari and Ando HWE-methodologies with alpha,beta-unsaturated aldehydes; unexpected results with stannyl substituted systems

Still-Gennari reactions have been carried out on a range of E- and Z-3-substituted propenals. In all cases, with the exception of Z-3-stannyl systems, good Z-stereoselectivity was observed. By contrast, the Ando procedure gives reasonable Z-stereoselectivity with all systems studied, including those...

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Main Authors: Franci, X, Martina, S, McGrady, J, Webb, MR, Donald, C, Taylor, R
Format: Journal article
Jezik:English
Izdano: 2003
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author Franci, X
Martina, S
McGrady, J
Webb, MR
Donald, C
Taylor, R
author_facet Franci, X
Martina, S
McGrady, J
Webb, MR
Donald, C
Taylor, R
author_sort Franci, X
collection OXFORD
description Still-Gennari reactions have been carried out on a range of E- and Z-3-substituted propenals. In all cases, with the exception of Z-3-stannyl systems, good Z-stereoselectivity was observed. By contrast, the Ando procedure gives reasonable Z-stereoselectivity with all systems studied, including those with a cis-disposed stannyl substituent. © 2003 Elsevier Ltd. All rights reserved.
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spelling oxford-uuid:fb5676fb-10d6-48db-8a2c-4b956c7dcfa72022-03-27T13:13:00ZA comparison of the Still-Gennari and Ando HWE-methodologies with alpha,beta-unsaturated aldehydes; unexpected results with stannyl substituted systemsJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:fb5676fb-10d6-48db-8a2c-4b956c7dcfa7EnglishSymplectic Elements at Oxford2003Franci, XMartina, SMcGrady, JWebb, MRDonald, CTaylor, RStill-Gennari reactions have been carried out on a range of E- and Z-3-substituted propenals. In all cases, with the exception of Z-3-stannyl systems, good Z-stereoselectivity was observed. By contrast, the Ando procedure gives reasonable Z-stereoselectivity with all systems studied, including those with a cis-disposed stannyl substituent. © 2003 Elsevier Ltd. All rights reserved.
spellingShingle Franci, X
Martina, S
McGrady, J
Webb, MR
Donald, C
Taylor, R
A comparison of the Still-Gennari and Ando HWE-methodologies with alpha,beta-unsaturated aldehydes; unexpected results with stannyl substituted systems
title A comparison of the Still-Gennari and Ando HWE-methodologies with alpha,beta-unsaturated aldehydes; unexpected results with stannyl substituted systems
title_full A comparison of the Still-Gennari and Ando HWE-methodologies with alpha,beta-unsaturated aldehydes; unexpected results with stannyl substituted systems
title_fullStr A comparison of the Still-Gennari and Ando HWE-methodologies with alpha,beta-unsaturated aldehydes; unexpected results with stannyl substituted systems
title_full_unstemmed A comparison of the Still-Gennari and Ando HWE-methodologies with alpha,beta-unsaturated aldehydes; unexpected results with stannyl substituted systems
title_short A comparison of the Still-Gennari and Ando HWE-methodologies with alpha,beta-unsaturated aldehydes; unexpected results with stannyl substituted systems
title_sort comparison of the still gennari and ando hwe methodologies with alpha beta unsaturated aldehydes unexpected results with stannyl substituted systems
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