Zobrazeno 1 - 10 of 131 pro vyhledávání: '"M. Knollmueller"'
1
Chiral linker 5: scope and limitations of arylsubstituted m-hydrobenzoins as solid supported open chain chiral auxiliaries for diastereoselective syntheses
Autor: Joachim Broeker, Peter Gaertner, M. Knollmueller
Publikováno v: Tetrahedron: Asymmetry. 20:273-287
The applicability of five aryl substituted m-hydrobenzoin ethers already tested in the L-Selectride® mediated stereoselective reduction of phenylglyoxylates as open chain chiral auxiliaries was further investigated via the α-alkylation of propionat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::834d3dc036481badbb86f435899945d2
https://doi.org/10.1016/j.tetasy.2009.02.004
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2
Chiral linker. Part 3: Synthesis and evaluation of aryl substituted m-hydrobenzoins as solid supported open chain chiral auxiliaries for the diastereoselective reduction of α-keto esters
Autor: M. Knollmueller, Peter Gaertner, Joachim Broeker
Publikováno v: Tetrahedron: Asymmetry. 17:2413-2429
Five partly novel aryl substituted m-hydrobenzoins were synthesized and the corresponding desymmetrized hydrobenzoin ethers evaluated as open chain chiral auxiliaries in the L-Selectride® mediated stereoselective reduction of phenylglyoxylates, resu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::48e3f1bc4339b98b795c006f715a09ed
https://doi.org/10.1016/j.tetasy.2006.08.017
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3
Chiral linker. Part 4: Diastereoselective addition of RZnX to α-keto esters using m-hydrobenzoin derived chiral auxiliaries in solution and on solid support and their application in the stereoselective synthesis of frontalin
Autor: Peter Gaertner, M. Knollmueller, Christian Schuster
Publikováno v: Tetrahedron: Asymmetry. 17:2430-2441
Two recently reported, m-hydrobenzoin derived open chain chiral auxiliaries, which were developed for application in either solution or immobilized on a solid support, were tested in the diastereoselective addition of RZnX to their corresponding phen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3594489dae6e0aa7d62534ecbf859e90
https://doi.org/10.1016/j.tetasy.2006.08.016
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4
Chiral linker. Part 2: Synthesis and evaluation of a novel, reusable solid-supported open chain chiral auxiliary derived from m-hydrobenzoin for the diastereoselective reduction of α-keto esters
Autor: Peter Gaertner, M. Knollmueller, Christian Schuster
Publikováno v: Tetrahedron: Asymmetry. 16:3211-3223
Three novel m -hydrobenzoin derived chiral hydrobenzoin mono -alkyl ethers were synthesized and evaluated as open chain chiral auxiliaries in the L-selectride R /ZnCl 2 mediated stereoselective reduction of their corresponding phenyl glyoxylates, res
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::89337f0aa8487e5b1530080b186bdd16
https://doi.org/10.1016/j.tetasy.2005.08.030
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5
Synthesis of novel chiral hydrobenzoin mono-tert-butyl ethers derived from m-hydrobenzoin and their application as chiral auxiliaries in the diastereoselective reduction of α-keto esters
Autor: M. Knollmueller, Peter Gaertner, Joachim Broeker, Christian Schuster
Publikováno v: Tetrahedron: Asymmetry. 16:2631-2647
Three m-hydrobenzoin derived chiral hydrobenzoin mono-tert-butyl ethers were synthesized by a new reaction pathway and tested as chiral auxiliaries in the L-selectride® mediated stereoselective reduction of their corresponding phenyl glyoxylates. As
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4c49e3c8a2b561b51c2f985090582384
https://doi.org/10.1016/j.tetasy.2005.06.033
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