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Showing 1 to 5 of 5 for “"Hydroxyalkylierung"”.
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Chirale Tris(amido)titanaallylsulfoximine: Stereoselektive Hydroxyalkylierung, Struktur und Dynamik
This thesis deals with stereoselective hydroxyalkylation reactions of E- and Z-configured allylic sulfoximines. Titanation of lithiated allylic sulfoximines with chlorotrisdiethylaminotitan and subsequent reaction of the resulting mono(2-alkenyl)tris(diethylamido)titan(IV)-complexes with aldehydes …
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Struktur, Hydroxyalkylierung und Aminoalkylierung von Titanaallylsulfoximinen: Enantioselektive Synthese ungesättigter Alpha-Aminosäuren
Structure, Hydroxyalkylation and Aminoalkylation of Titanaallylsulfoximines: Enantioselective Synthesis of Unsaturated alpha-Amino Acids Enantiopure E- and Z-allylic sulfoximines were lithiated and transmetallated with ClxTi(OR)4-x to give bis(2-alkenyl)titanium(IV)-complexes. These complexes …
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Asymmetrische Synthese und stereoselektive Substitution allylischer Sulfoximin-funktionalisierter Homoallylalkohole
Enantiopure acyclic (E)- and (Z)-configured allylic sulfoximines have been synthesized from N,S-dimethyl-S-phenylsulfoximine and aldehydes via the addition-elimination-isomerization route. Titanation of lithiated (E)- and (Z)-configured allylic sulfoximines with Chlortrisdiethylanimotitan and …
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Asymmetrische Synthese funktionalisierter Homoallyl- und Homopropargylalkohole mittels der Sulfoximin-Route
This dissertation describes new methods of asymmetric synthesis of diastereomeric and enantiomeric pure allylic alcohols. Via the sulfoximine-route by Gais et al. new chiral homoallyllic alcohols were synthesized. Elimination of the sulfoximine-group lead to optically pure homopropargylic alcohols. …