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A Cyclic Continuous Process for Converting Conglomerates into Optically Pure Enantiomers by Crystallization and Dissolution with the Assistance of ‘Tailor-made’ Polymers

Tetrahedron, 2000-09, Vol.56 (36), p.6645-6649

2000

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Enzymatic reduction of α-keto acids leading to l-amino acids, d- or l-hydroxy acids

Journal of biotechnology, 1997-02, Vol.53 (1), p.29-39

1997

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Structure and dynamics of synthetic O-glycosylated cyclopeptide in solution determined by NMR spectroscopy and MD calculations

Journal of the American Chemical Society, 1992-06, Vol.114 (12), p.4805-4818

1992

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Solution structure of a synthetic N-glycosylated cyclic hexapeptide determined by NMR spectroscopy and MD calculations

Journal of the American Chemical Society, 1991-09, Vol.113 (20), p.7550-7563

1991

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ICDD Annual Spring Meetings

Powder diffraction, 2015-09, Vol.30 (3), p.303-317

2015

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Synthesis and use of enantiomerically pure tert-leucine

Tetrahedron: asymmetry, 1995-12, Vol.6 (12), p.2851-2888

1995

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Kinetics of Peptide Amidase and its Application for the Resolution of Racemates

Biocatalysis and biotransformation, 1997, Vol.15 (3), p.205-219

1997

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2012 ICDD Annual Spring Meetings

Powder diffraction, 2012-06, Vol.27 (2), p.140-146

Kozul, Tess

2012

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Process for the preparation of 2-( S)-piperazinecarboxylic acid by continuous resolution via diastereomeric salt pairs

Tetrahedron: asymmetry, 1997-04, Vol.8 (7), p.979-982

1997

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Synthese von 2-Desoxy-α-O-glycopeptiden mit dem N-Iodsuccinimid-(NIS-) Verfahren

Liebigs Annalen der Chemie, 1991-08, Vol.1991 (8), p.727-744

1991

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Synthesis of C-Glycopeptides via Free Radical Addition of Glycosyl Bromides to Dehydroalanine Derivatives

Angewandte Chemie (International ed.), 1992-07, Vol.31 (7), p.902-904

1992

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ChemInform Abstract: Synthesis and Use of Enantiomerically Pure tert-Leucine

ChemInform, 1996-04, Vol.27 (16), p.no-no

1996

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Chemoenzymatische Synthesen von D-ω-Ureidoaminosäuren

Angewandte Chemie, 1991-06, Vol.103 (6), p.704-706

1991

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TMS Triflate-Promoted O-Glycosylation of Amino Acids and Peptides by L-Acosaminal and L-Ristosaminal

Liebigs Annalen der Chemie, 1994-08, Vol.1994 (8), p.811-816

1994

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Synthese von O-(α-Glyco)peptiden mit dem N-Iodsuccinimid-Verfahren

Angewandte Chemie, 1987-09, Vol.99 (9), p.919-921

1987

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Structure and dynamics of a synthetic O-glycosylated cylopeptide in solution determined by NMR spectroscopy and MD calculations

Journal of the American Chemical Society, 1992, Vol.114 (12), p.4805-4818

1992

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ChemInform Abstract: Chiral Amino Acids. A Versatile Tool in the Synthesis of Pharmaceuticals and Fine Chemicals

ChemInform, 1995-04, Vol.26 (15), p.no-no

1995

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Facile Synthesis of a β(1-3)-Linked gal-galactal Disaccharide and Its Use in N-Iodosuccinimide-Activated O-Glycopeptide Synthesis

Angewandte Chemie (International ed.), 1990-04, Vol.29 (4), p.425-427

1990

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Synthesis of 2-deoxy- alpha -O-glycopeptides by the N-iodosuccinimide (NIS) procedure

Liebigs Annalen der Chemie, 1991-08, Vol.1991 (8), p.727-744

1991

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Chiral synthesis as an approach to key drug intermediates

Manufacturing chemist (London : 1981), 1996-01, Vol.67 (1), p.16

1996

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ChemInform Abstract: Synthesis of 2-Deoxy-α-O-glycopeptides by the N-Iodosuccinimide ( NIS) Procedure

ChemInform, 1991-10, Vol.22 (42), p.no-no

1991

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ChemInform Abstract: Process for the Preparation of 2-(S)-Piperazinecarboxylic Acid by Continuous Resolution via Diastereomeric Salt Pairs

ChemInform, 1997-08, Vol.28 (33), p.no-no

1997

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Synthesis of O-(α-Glyco)peptides by the N-Iodosuccinimide Procedure

Angewandte Chemie (International ed.), 1987-09, Vol.26 (9), p.888-890

1987

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ChemInform Abstract: A Cyclic Continuous Process for Converting Conglomerates into Optically Pure Enantiomers by Crystallization and Dissolution with the Assistance of "Tailor-Made" Polymers

ChemInform, 2000-12, Vol.31 (49), p.no-no

2000

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ChemInform Abstract: TMS Triflate-Promoted O-Glycosylation of Amino Acids and Peptides by L- Acosaminal and L-Ristosaminal

ChemInform, 1995-01, Vol.26 (1), p.no-no

1995

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A Cyclic Continuous Process for Converting Conglomerates into Optically Pure Enantiomers by Crystallization and Dissolution with the Assistance of ‘Tailor-made’ Polymers

Enzymatic reduction of α-keto acids leading to l-amino acids, d- or l-hydroxy acids

Structure and dynamics of synthetic O-glycosylated cyclopeptide in solution determined by NMR spectroscopy and MD calculations

Solution structure of a synthetic N-glycosylated cyclic hexapeptide determined by NMR spectroscopy and MD calculations

ICDD Annual Spring Meetings

Synthesis and use of enantiomerically pure tert-leucine

Kinetics of Peptide Amidase and its Application for the Resolution of Racemates

2012 ICDD Annual Spring Meetings

Process for the preparation of 2-( S)-piperazinecarboxylic acid by continuous resolution via diastereomeric salt pairs

Synthese von 2-Desoxy-α-O-glycopeptiden mit dem N-Iodsuccinimid-(NIS-) Verfahren

Synthesis of C-Glycopeptides via Free Radical Addition of Glycosyl Bromides to Dehydroalanine Derivatives

ChemInform Abstract: Synthesis and Use of Enantiomerically Pure tert-Leucine

Chemoenzymatische Synthesen von D-ω-Ureidoaminosäuren

TMS Triflate-Promoted O-Glycosylation of Amino Acids and Peptides by L-Acosaminal and L-Ristosaminal

Synthese von O-(α-Glyco)peptiden mit dem N-Iodsuccinimid-Verfahren

Structure and dynamics of a synthetic O-glycosylated cylopeptide in solution determined by NMR spectroscopy and MD calculations

ChemInform Abstract: Chiral Amino Acids. A Versatile Tool in the Synthesis of Pharmaceuticals and Fine Chemicals

Facile Synthesis of a β(1-3)-Linked gal-galactal Disaccharide and Its Use in N-Iodosuccinimide-Activated O-Glycopeptide Synthesis

Synthesis of 2-deoxy- alpha -O-glycopeptides by the N-iodosuccinimide (NIS) procedure

Chiral synthesis as an approach to key drug intermediates

ChemInform Abstract: Synthesis of 2-Deoxy-α-O-glycopeptides by the N-Iodosuccinimide ( NIS) Procedure

ChemInform Abstract: Process for the Preparation of 2-(S)-Piperazinecarboxylic Acid by Continuous Resolution via Diastereomeric Salt Pairs

Synthesis of O-(α-Glyco)peptides by the N-Iodosuccinimide Procedure

ChemInform Abstract: A Cyclic Continuous Process for Converting Conglomerates into Optically Pure Enantiomers by Crystallization and Dissolution with the Assistance of "Tailor-Made" Polymers

ChemInform Abstract: TMS Triflate-Promoted O-Glycosylation of Amino Acids and Peptides by L- Acosaminal and L-Ristosaminal

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