Year |
Citation |
Score |
2019 |
Denner C, Gintner M, Kählig H, Schmid W. Indium-mediated C-allylation of melibiose. Beilstein Journal of Organic Chemistry. 15: 2458-2464. PMID 31666880 DOI: 10.3762/Bjoc.15.238 |
0.34 |
|
2019 |
Gintner M, Yoneda Y, Schmölzer C, Denner C, Kählig H, Schmid W. A versatile de novo synthesis of legionaminic acid and 4-epi-legionaminic acid starting from d-serine. Carbohydrate Research. 474: 34-42. PMID 30711766 DOI: 10.1016/J.Carres.2019.01.009 |
0.4 |
|
2019 |
Gintner M, Denner C, Schmölzer C, Fischer M, Frühauf P, Kählig H, Schmid W. Synthesis of 3-deoxy-2-uloses via the indium-mediated allylation reaction Monatshefte FüR Chemie - Chemical Monthly. 150: 849-860. DOI: 10.1007/S00706-019-02438-Y |
0.406 |
|
2018 |
Riedl B, Schmid W. A stereoselective and flexible synthesis to access both enantiomers of -acetylgalactosamine and peracetylated -acetylidosamine. Beilstein Journal of Organic Chemistry. 14: 856-860. PMID 29719580 DOI: 10.3762/Bjoc.14.71 |
0.349 |
|
2017 |
Riedl B, Schmid W. A concise route to access C-glycosidic tetrazolyl analogues of Kdo as bioisosteres. Carbohydrate Research. 456: 30-34. PMID 29272779 DOI: 10.1016/J.Carres.2017.12.006 |
0.396 |
|
2015 |
Schörghuber J, Sára T, Bisaccia M, Schmid W, Konrat R, Lichtenecker RJ. Novel approaches in selective tryptophan isotope labeling by using Escherichia coli overexpression media. Chembiochem : a European Journal of Chemical Biology. 16: 746-51. PMID 25703586 DOI: 10.1002/Cbic.201402677 |
0.318 |
|
2015 |
Albler C, Schmid W. From Amino Acids to Fluorine-Containing Carbohydrates: De Novo Synthesis of 2-Amino-4-Fluoroxylose and -lyxose European Journal of Organic Chemistry. DOI: 10.1002/Ejoc.201403532 |
0.394 |
|
2014 |
Albler C, Hollaus R, Kählig H, Schmid W. Indium-mediated allylation in carbohydrate synthesis: A short and efficient approach towards higher 2-acetamido-2-deoxy sugars. Beilstein Journal of Organic Chemistry. 10: 2230-4. PMID 25246982 DOI: 10.3762/Bjoc.10.231 |
0.358 |
|
2014 |
Albler C, Schmid W. Synthetic routes towards fluorine-containing amino sugars: Synthesis of fluorinated analogues of tomosamine and 4-amino-4-deoxyarabinose European Journal of Organic Chemistry. 2014: 2451-2459. DOI: 10.1002/Ejoc.201301614 |
0.365 |
|
2013 |
Lichtenecker RJ, Weinhäupl K, Schmid W, Konrat R. α-Ketoacids as precursors for phenylalanine and tyrosine labelling in cell-based protein overexpression. Journal of Biomolecular Nmr. 57: 327-31. PMID 24264768 DOI: 10.1007/S10858-013-9796-9 |
0.341 |
|
2013 |
Schmölzer C, Nowikow C, Kählig H, Schmid W. Gram scale de novo synthesis of 2,4-diacetamido-2,4,6-trideoxy-D-galactose. Carbohydrate Research. 367: 1-4. PMID 23266666 DOI: 10.1016/J.Carres.2012.11.019 |
0.344 |
|
2011 |
Fischer M, Kählig H, Schmid W. Gram scale synthesis of 3-fluoro-1-hydroxyacetone phosphate: a novel donor substrate in rabbit muscle aldolase-catalyzed aldol reactions. Chemical Communications (Cambridge, England). 47: 6647-9. PMID 21562661 DOI: 10.1039/C1Cc11579K |
0.302 |
|
2011 |
Fischer M, Schmölzer C, Nowikow C, Schmid W. Indium-Mediated Allenylation of Aldehydes and Its Application in Carbohydrate Chemistry: Efficient Synthesis of D-Ribulose and 1-Deoxy-D-ribulose (Eur. J. Org. Chem. 9/2011) European Journal of Organic Chemistry. 2011: n/a-n/a. DOI: 10.1002/Ejoc.201190018 |
0.356 |
|
2011 |
Fischer M, Schmölzer C, Nowikow C, Schmid W. Indium-Mediated Allenylation of Aldehydes and Its Application in Carbohydrate Chemistry: Efficient Synthesis of D-Ribulose and 1-Deoxy-D-ribulose European Journal of Organic Chemistry. 2011: 1645-1651. DOI: 10.1002/Ejoc.201001443 |
0.375 |
|
2010 |
Schmölzer C, Fischer M, Schmid W. Permanganate Oxidation Revisited: Synthesis of 3-Deoxy-2-uloses via Indium-Mediated Chain Elongation of Carbohydrates European Journal of Organic Chemistry. 2010: 4886-4892. DOI: 10.1002/Ejoc.201000623 |
0.374 |
|
2008 |
Schmid W, Nagl M, Panuschka C, Barta A. The BF3×OEt2-Assisted Conversion of Nitriles into Thioamides with Lawesson’s Reagent Synthesis. 2008: 4012-4018. DOI: 10.1055/S-0028-1083253 |
0.31 |
|
2007 |
Fischer M, Kloiber K, Häusler J, Ledolter K, Konrat R, Schmid W. Synthesis of a 13C-methyl-group-labeled methionine precursor as a useful tool for simplifying protein structural analysis by NMR spectroscopy. Chembiochem : a European Journal of Chemical Biology. 8: 610-2. PMID 17328009 DOI: 10.1002/Cbic.200600551 |
0.32 |
|
2007 |
Fischer M, Kloiber K, Häusler J, Ledolter K, Konrat R, Schmid W. Cover Picture: Synthesis of a13C-Methyl-Group-Labeled Methionine Precursor as a Useful Tool for Simplifying Protein Structural Analysis by NMR Spectroscopy (ChemBioChem 6/2007) Chembiochem. 8: 581-581. DOI: 10.1002/Cbic.200790013 |
0.301 |
|
2006 |
Kawada T, Yoneda Y, Asano R, Kan-no I, Schmid W. Synthesis of plantamajoside, a bioactive dihydroxyphenylethyl glycoside from Plantago major L. Holzforschung. 60: 492-497. DOI: 10.1515/Hf.2006.081 |
0.351 |
|
2004 |
Lichtenecker R, Ludwiczek ML, Schmid W, Konrat R. Simplification of protein NOESY spectra using bioorganic precursor synthesis and NMR spectral editing. Journal of the American Chemical Society. 126: 5348-9. PMID 15113192 DOI: 10.1021/Ja049679N |
0.36 |
|
2002 |
Wenzl I, Neuwirth N, Hedenetz AG, Fiedler C, Streicher H, Unger FM, Schmid W. Synthesis of Sulfur-Containing Analogues of ΑGalNAc (Tn-Antigen) and ΒGal1,3ΑGalNAc (T-Antigen) Monatshefte F?R Chemie / Chemical Monthly. 133: 531-540. DOI: 10.1007/978-3-7091-6130-2_12 |
0.331 |
|
1999 |
Klaps E, Schmid W. Carboindation of Carbon−Carbon Triple Bonds: Regioselective Indium-Mediated Allylation of Functionalized Alkynes and Transformation into Halogen-Substituted 1,4-Dienes The Journal of Organic Chemistry. 64: 7537-7546. DOI: 10.1021/Jo9908593 |
0.358 |
|
1999 |
Wenzl I, Kählig H, Unger FM, Schmid W. A Novel Approach to β-(1→4)-Linked Thiodisaccharides Starting from Disulfide Sugars Monatshefte FüR Chemie / Chemical Monthly. 130: 1137-1145. DOI: 10.1007/Pl00010292 |
0.334 |
|
1995 |
Binder WH, Kählig H, Schmid W. Galactosylation by use of β-galactosidase: Enzymatic syntheses of disaccharide nucleosides Tetrahedron: Asymmetry. 6: 1703-1710. DOI: 10.1016/0957-4166(95)00216-C |
0.361 |
|
1994 |
Binder WH, Kählig H, Schmid W. Galactosylation by use of β-galactosidase: Chemo-enzymatic syntheses of di- and trisaccharides Tetrahedron. 50: 10407-10418. DOI: 10.1016/S0040-4020(01)89581-8 |
0.359 |
|
1994 |
Binder WH, Prenner RH, Schmid W. Indium-mediated allylation of aldehydes: A convenient route to 2-deoxy and 2,6-dideoxy carbohydrates Tetrahedron. 50: 749-758. DOI: 10.1016/S0040-4020(01)80790-0 |
0.323 |
|
1994 |
Prenner RH, Binder WH, Schmid W. Indium-assisted allylation in carbohydrate chemistry: A convenient route toD-glycero-D-galacto- andD-glycero-L-galacto-heptose Liebigs Annalen Der Chemie. 1994: 73-78. DOI: 10.1002/Jlac.199419940113 |
0.418 |
|
1993 |
Maliakel BP, Schmid W. Total Synthesis of Sphydrofuran Journal of Carbohydrate Chemistry. 12: 415-424. DOI: 10.1080/07328309308019397 |
0.374 |
|
1993 |
Kim E, Gordon DM, Schmid W, Whitesides GM. Tin- and indium-mediated allylation in aqueous media: application to unprotected carbohydrates The Journal of Organic Chemistry. 58: 5500-5507. DOI: 10.1021/Jo00072A038 |
0.452 |
|
1993 |
Schmid W, Avila LZ, Williams KW, Whitesides GM. Synthesis of methyl α-sialosides N-substituted with large alkanoyl groups, and investigation of their inhibition of agglutination of erythrocytes by influenza A virus Bioorganic and Medicinal Chemistry Letters. 3: 747-752. DOI: 10.1016/S0960-894X(01)81267-1 |
0.354 |
|
1992 |
Kelm S, Paulson JC, Rose U, Brossmer R, Schmid W, Bandgar BP, Schreiner E, Hartmann M, Zbiral E. Use of sialic acid analogues to define functional groups involved in binding to the influenza virus hemagglutinin. European Journal of Biochemistry / Febs. 205: 147-53. PMID 1555576 DOI: 10.1111/J.1432-1033.1992.Tb16762.X |
0.532 |
|
1992 |
Maliakel BP, Schmid W. Chemo-enzymatic synthesis of natural products: synthesis of sphydrofuran Tetrahedron Letters. 33: 3297-3300. DOI: 10.1016/S0040-4039(00)92071-9 |
0.343 |
|
1992 |
Schmid W, Heidlas J, Mathias JP, Whitesides GM. Chemo-enzymatische Synthese von Kohlenhydraten: Die Herstellung vonL-Xylose und 2-Desoxy-L-xylo-hexose Liebigs Annalen Der Chemie. 1992: 95-97. DOI: 10.1002/Jlac.199219920119 |
0.454 |
|
1991 |
Shames SL, Simon ES, Christopher CW, Schmid W, Whitesides GM, Yang LL. CMP-N-acetylneuraminic acid synthetase of Escherichia coli: high level expression, purification and use in the enzymatic synthesis of CMP-N-acetylneuraminic acid and CMP-neuraminic acid derivatives. Glycobiology. 1: 187-91. PMID 1823161 DOI: 10.1093/Glycob/1.2.187 |
0.381 |
|
1991 |
Schmid W, Whitesides GM. Carbon-carbon bond formation in aqueous ethanol: diastereoselective transformation of unprotected carbohydrates to higher carbon sugars using allyl bromide and tin metal Journal of the American Chemical Society. 113: 6674-6675. DOI: 10.1021/Ja00017A049 |
0.36 |
|
1990 |
Schmid W, Whitesides GM. A new approach to cyclitols based on rabbit-muscle aldolase (RAMA) Journal of the American Chemical Society. 112: 9670-9671. DOI: 10.1021/Ja00182A054 |
0.354 |
|
1990 |
Bandgar BP, Hartmann M, Schmid W, Zbiral E. Structural variations ofN-acetylneuraminic acid, 18. Synthesis of the side chain stereo and deoxy analogs of 5-acetamido-2,6-anhydro-3,5-dideoxy-D-erythro-L-manno-nononic acid Liebigs Annalen Der Chemie. 1990: 1185-1195. DOI: 10.1002/Jlac.1990199001216 |
0.566 |
|
1988 |
Schmid W, Christian R, Zbiral E. Synthesis of both epimeric 2-deoxy-n-acetylneuraminic acids and their behaviour towards CMP-sialate synthetase-a comparison with 2-β-methylketoside of n-acetylneuraminic acid Tetrahedron Letters. 29: 3643-3646. DOI: 10.1016/S0040-4039(00)82143-7 |
0.557 |
|
1988 |
Salunkhe M, Hartmann M, Schmid W, Zbiral E. Structural variations ofN-acetylneuraminic acid, 9. A new useful approach to the epimers at C-7 and C-7,8 ofN-acetylneuraminic acid Liebigs Annalen Der Chemie. 1988: 187-189. DOI: 10.1002/Jlac.198819880215 |
0.547 |
|
1987 |
Zbiral E, Phadtare S, Schmid W. Strukturelle Abwandlungen anN-Acetylneuraminsäure, 6. Synthesen von 7-Oxo- und 8-Oxo-N-acetylneuraminsäure-Derivaten Liebigs Annalen Der Chemie. 1987: 39-43. DOI: 10.1002/Jlac.198719870107 |
0.525 |
|
1986 |
Schmid W, Zbiral E, Christian R, Schulz G. Strukturelle Abwandlungen anN-Acetylneuraminsäure, 5(1) Zur Transformation der Carboxylgruppe vonN-Acetylneuraminsäure in die Tetrazol-Gruppe Liebigs Annalen Der Chemie. 1986: 2104-2111. DOI: 10.1002/Jlac.198619861205 |
0.573 |
|
1985 |
Robien W, Schmid W, Zbiral E. Investigation of the conformation in solution of some derivatives of N-acetylneuramino-1,4-lactone diethyl dithioacetal by one- and two-dimensional n.m.r. techniques Carbohydrate Research. 141: 21-28. DOI: 10.1016/S0008-6215(00)90751-1 |
0.514 |
|
1985 |
Zbiral E, Schmid W. Transformations on the diethyldithioketal of N-acetylneuraminic acid-γ-lactone | Strukturelle Abwandlungen an N-Acetylneuraminsäure, 4. Mitt. Transformationen am Diethyl-dithioketal des N-Acetylneuraminsäure-γ-lactons Monatshefte FüR Chemie Chemical Monthly. 116: 253-262. DOI: 10.1007/Bf00798461 |
0.556 |
|
1983 |
Schmid W, Zbiral E. A new approach to 3-acetylamino-3-desoxy-d-galactose | Strukturelle Abwandlungen an Kohlenhydraten, 7. Mitt. - Ein neuer Zugang zu 3-Acetylamino-3-desoxy-D-galaktose Monatshefte FüR Chemie Chemical Monthly. 114: 1253-1258. DOI: 10.1007/Bf00799940 |
0.509 |
|
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