ChemInform Abstract: Reversed Stereochemical Control in the Presence of CeCl 3 and TiCl 4 in the Lewis Acid Mediated Reduction of α‐Alkyl‐β‐keto Esters by Metal Hydrides. A General Methodology for the Diastereoselective Synthesis of syn‐ and anti‐α‐Alkyl‐β‐hydroxy Esters

ChemInform Abstract: Reversed Stereochemical Control in the Presence of CeCl 3 and TiCl 4 in the Lewis Acid Mediated Reduction of α‐Alkyl‐β‐keto Esters by Metal Hydrides. A General Methodology for the Diastereoselective Synthesis of syn‐ and anti‐α‐Alkyl‐β‐hydroxy Esters

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “Refer...

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Veröffentlicht in:ChemInform 1999-08, Vol.30 (32)
Hauptverfasser: Marcantoni, Enrico, Alessandrini, Sara, Malavolta, Marco, Bartoli, Giuseppe, Bellucci, Maria Cristina, Sambri, Letizia, Dalpozzo, Renato
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container_issue 32
container_start_page
container_title ChemInform
container_volume 30
creator Marcantoni, Enrico
Alessandrini, Sara
Malavolta, Marco
Bartoli, Giuseppe
Bellucci, Maria Cristina
Sambri, Letizia
Dalpozzo, Renato
description ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
doi_str_mv 10.1002/chin.199932029
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source Wiley Online Library Journals Frontfile Complete
title ChemInform Abstract: Reversed Stereochemical Control in the Presence of CeCl 3 and TiCl 4 in the Lewis Acid Mediated Reduction of α‐Alkyl‐β‐keto Esters by Metal Hydrides. A General Methodology for the Diastereoselective Synthesis of syn‐ and anti‐α‐Alkyl‐β‐hydroxy Esters
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