ChemInform Abstract: Diastereoselective Synthesis of Substituted Tetrahydroquinoline-4-carboxylic Esters by a Tandem Reduction-Reductive Amination Reaction

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

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Veröffentlicht in:	ChemInform 2001-09, Vol.32 (36), p.no-no
Hauptverfasser:	Bunce, Richard A., Herron, Derrick M., Johnson, Lara B., Kotturi, Sharadsrikar V.
Format:	Artikel
Sprache:	eng
Schlagworte:	amination amination, N‐alkylation, N‐arylation diastereoselective syntheses diastereoselective syntheses, enantioselective syntheses (incl. ci/trans‐isomerism) enantioselective syntheses (incl. ci/trans-isomerism) hydrogenation N-alkylation N-arylation ozonolysis quinoline derivatives reduction reduction, hydrogenation ring closure reactions
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description	ChemInform is a weekly ing Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform 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.200136139
format	Article
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subjects	amination amination, N‐alkylation, N‐arylation diastereoselective syntheses diastereoselective syntheses, enantioselective syntheses (incl. ci/trans‐isomerism) enantioselective syntheses (incl. ci/trans-isomerism) hydrogenation N-alkylation N-arylation ozonolysis quinoline derivatives reduction reduction, hydrogenation ring closure reactions
title	ChemInform Abstract: Diastereoselective Synthesis of Substituted Tetrahydroquinoline-4-carboxylic Esters by a Tandem Reduction-Reductive Amination Reaction
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