Lithiated Dimethoxymethyl Diphenyl Phosphine Oxide, A Versatile Formiate Carbanion Equivalent
Abstract Aldehydes are homologated to the corresponding α-hydroxy methyl esters using lithiated dimethoxymethyl diphenyl phosphine oxide. The primary addition product of this Horner-Wittig process collapses to the corresponding α-hydroxy ester under proton-catalyzed conditions.
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Veröffentlicht in: | Synlett 2002, Vol.2002 (3), p.525-527 |
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container_issue | 3 |
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container_title | Synlett |
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creator | Monenschein, Holger Brünjes, Marco Kirschning, Andreas |
description | Abstract
Aldehydes are homologated to the corresponding α-hydroxy methyl esters using lithiated dimethoxymethyl diphenyl phosphine oxide. The primary addition product of this Horner-Wittig process collapses to the corresponding α-hydroxy ester under proton-catalyzed conditions. |
doi_str_mv | 10.1055/s-2002-20486 |
format | Article |
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Aldehydes are homologated to the corresponding α-hydroxy methyl esters using lithiated dimethoxymethyl diphenyl phosphine oxide. The primary addition product of this Horner-Wittig process collapses to the corresponding α-hydroxy ester under proton-catalyzed conditions.</abstract><doi>10.1055/s-2002-20486</doi><tpages>3</tpages></addata></record> |
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identifier | ISSN: 0936-5214 |
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issn | 0936-5214 1437-2096 |
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title | Lithiated Dimethoxymethyl Diphenyl Phosphine Oxide, A Versatile Formiate Carbanion Equivalent |
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