Publikation: Asymmetric Synthesis of Diastereomerically and Enantiomerically Pure 3-Substituted (2R,3S)-Serine Methyl Esters
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1991
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Published
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Liebigs Annalen der Chemie. 1991, 1991(11), pp. 1207-1209. ISSN 0170-2041. eISSN 1099-0690. Available under: doi: 10.1002/jlac.1991199101206
Zusammenfassung
The titanium derivative 2 of the bislactim ether 1 of cyclo(-LVal-Gly-) reacts with aldehydes and ketones 3 highly diastereoselectively to give the syn-addition products 4. Upon hydrolysis with diluted trifluoroacetic acid the compounds 4 yield besides methyl L-valinate the (2R,BS)-threo-serinme ethyl esters 5.
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Fachgebiet (DDC)
540 Chemie
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Serine, 3-substituted, methyl esters, Bislactim ether method
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BEULSHAUSEN, Tessa, Ulrich GROTH, Ulrich SCHÖLLKOPF, 1991. Asymmetric Synthesis of Diastereomerically and Enantiomerically Pure 3-Substituted (2R,3S)-Serine Methyl Esters. In: Liebigs Annalen der Chemie. 1991, 1991(11), pp. 1207-1209. ISSN 0170-2041. eISSN 1099-0690. Available under: doi: 10.1002/jlac.1991199101206BibTex
@article{Beulshausen1991Asymm-9734,
year={1991},
doi={10.1002/jlac.1991199101206},
title={Asymmetric Synthesis of Diastereomerically and Enantiomerically Pure 3-Substituted (2R,3S)-Serine Methyl Esters},
number={11},
volume={1991},
issn={0170-2041},
journal={Liebigs Annalen der Chemie},
pages={1207--1209},
author={Beulshausen, Tessa and Groth, Ulrich and Schöllkopf, Ulrich}
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<dcterms:abstract xml:lang="eng">The titanium derivative 2 of the bislactim ether 1 of cyclo(-LVal-Gly-) reacts with aldehydes and ketones 3 highly diastereoselectively to give the syn-addition products 4. Upon hydrolysis with diluted trifluoroacetic acid the compounds 4 yield besides methyl L-valinate the (2R,BS)-threo-serinme ethyl esters 5.</dcterms:abstract>
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