Readily Accessible Chiral Diene Ligands for Rh-Catalyzed Enantioselective Conjugate Additions of Boronic Acids
Enabled by the broad scope of the Pd-catalyzed asymmetric alkylation of meso- and d,l-divinylethylene carbonate, several chiral diene ligands were prepared in two steps from commercial materials. Subsequently, these ligands were evaluated in the Rh-catalyzed asymmetric conjugate addition of boronic...
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Veröffentlicht in: | Organic letters 2011-09, Vol.13 (17), p.4566-4569 |
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creator | Trost, Barry M Burns, Aaron C Tautz, Thomas |
description | Enabled by the broad scope of the Pd-catalyzed asymmetric alkylation of meso- and d,l-divinylethylene carbonate, several chiral diene ligands were prepared in two steps from commercial materials. Subsequently, these ligands were evaluated in the Rh-catalyzed asymmetric conjugate addition of boronic acids to enones. |
doi_str_mv | 10.1021/ol201754c |
format | Article |
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Lett</addtitle><description>Enabled by the broad scope of the Pd-catalyzed asymmetric alkylation of meso- and d,l-divinylethylene carbonate, several chiral diene ligands were prepared in two steps from commercial materials. 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source | MEDLINE; American Chemical Society Journals |
subjects | Boronic Acids - chemistry Catalysis Cycloparaffins - chemistry Hydrocarbons, Cyclic - chemical synthesis Hydrocarbons, Cyclic - chemistry Ligands Molecular Structure Organometallic Compounds - chemistry Palladium - chemistry Rhodium - chemistry Stereoisomerism |
title | Readily Accessible Chiral Diene Ligands for Rh-Catalyzed Enantioselective Conjugate Additions of Boronic Acids |
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