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Enzymatic synthesis of the delicious peptide fragments in eutectic mixtures

Journal of agricultural and food chemistry, 1995-09, Vol.43 (9), p.2536-2541

1995

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Biologically active peptides and enzymatic approaches to their production

Enzyme and Microbial Technology, 1996-02, Vol.18 (3), p.162-183

1996

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Optimization and kinetic studies of the enzymatic synthesis of Ac-Phe-Leu-NH2 in reversed micelles

Enzyme and microbial technology, 1992-02, Vol.14 (2), p.117-124

1992

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Ethyl acetate modified AOT water-in-oil microemulsions for the α-chymotrypsin catalyzed synthesis of a model dipeptide derivative

Colloids and surfaces. A, Physicochemical and engineering aspects, 1995-03, Vol.96 (1), p.47-52

1995

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Hydrolysis of N-protected amino acid allyl esters by enzymatic catalysis

Biotechnology letters, 1989-06, Vol.11 (6), p.393-396

1989

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Racemization free coupling of peptide segments : synthesis of an insect neuropeptide

International journal of peptide and protein research, 1992-06, Vol.39 (6), p.528-532

1992

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Enzymatic peptide fragment condensation. Choice of reaction media for the synthesis of an insect neuropeptide derivative

Biotechnology techniques, 1992, Vol.6 (1), p.69-72

1992

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Contribution of C-tail residues of potato carboxypeptidase inhibitor to the binding to carboxypeptidase A. A mutagenesis analysis

European journal of biochemistry, 2000-03, Vol.267 (5), p.1502-1509

2000

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Ethyl acetate modified AOT water-in-oil microemulssions for the α-chymotrypsin catalyzed synthesis of a model dipeptide derivative

Colloids and surfaces. A, Physicochemical and engineering aspects, 1995, Vol.96 (1-2), p.47-52

1995

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Arenesulphonyltriazolides as condensing reagents in solid phasepeptide synthesis

Tetrahedron letters, 1990, Vol.31 (13), p.1915-1918

1990

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Anchoring of Fmoc-amino acids to hydroxymethyl resins

International Journal of Peptide and Protein Research, 1989-05, Vol.33 (5), p.386-390

1989

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Arenesulphonyltriazolides as condensing reagents in solid phase peptide synthesis

Tetrahedron letters, 1990, Vol.31 (13), p.1915-1918

1990

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Optimization and kinetic studies of the enzymatic synthesis of Ac-Phe-Leu-NH 2 in reversed micelles

Enzyme and microbial technology, 1992, Vol.14 (2), p.117-124

1992

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Application of empirical design methodologies to the study of the influence of reaction conditions and N-α-protecting group structure on the enzymatic X-Phe-Leu-NH2 dipeptide synthesis in buffer/dimethylformamide solvent systems

Biotechnology and bioengineering, 1992-03, Vol.39 (5), p.539-549

1992

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New enzymatic approach to the synthesis of convenient aspartic acid intermediates in peptide chemistry. Synthesis of n-benzyloxycarbonyl-l-aspartic acid β-allyl ester

Tetrahedron, 1989, Vol.45 (23), p.7421-7426

1989

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Application of empirical design methodologies to the study of the influence of reaction conditions and N-α-protecting group structure on the enzymatic X-Phe-Leu-NH2 dipeptide synthesis in buffer/dimethylformamide solvents systems

Biotechnology and bioengineering, 1992-03, Vol.39 (5), p.539-549

1992

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Application of empirical design methodologies to the study of the influence of reaction conditions and N-alpha-protecting group structure on the enzymatic X-Phe-Leu-NH(2) dipeptide synthesis in buffer/dimethylformamide solvents systems

Biotechnology and bioengineering, 1992-03, Vol.39 (5), p.539-549

1992

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New enzymatic approach to the synthesis of convenient aspartic acid intermediates in peptide chemistry: synthesis of N-benzoyloxycarbonyl-L-aspartic acid β-allyl ester

Tetrahedron, 1989, Vol.45 (23), p.7421-7426

1989

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Application of empirical design methodologies to the study of the influence of reaction conditions and N ‐α‐protecting group structure on the enzymatic X‐Phe‐Leu‐NH 2 dipeptide synthesis in buffer/dimethylformamide solvents systems

Biotechnology and bioengineering, 1992-03, Vol.39 (5), p.539-549

1992

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Racemization free coupling of peptide segments

International Journal of Peptide and Protein Research, 1992-06, Vol.39 (6), p.528-532

1992

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ChemInform Abstract: Arenesulfonyltriazolides as Condensing Reagents in Solid Phase Peptide Synthesis

ChemInform, 1991-02, Vol.22 (5), p.no-no

1991

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Online coupled regional meteorology chemistry models in Europe: current status and prospects

Atmospheric chemistry and physics, 2014-01, Vol.14 (1), p.317-398

2014

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A new NMVOC speciated inventory for a reactivity-based approach to support ozone control strategies in Spain

The Science of the total environment, 2023-04, Vol.867, p.161449, Article 161449

2023

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Improved method for the synthesis of o-glycosylated Fmoc amino acids to be used in solid-phase glycopeptide synthesis (Fmoc = fluoren-9-ylmethoxycarbonyl)

Journal of the Chemical Society. Chemical communications, 1990 (14), p.965-967

1990

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ChemInform Abstract: Improved Method for the Synthesis of O-Glycosylated Fmoc Amino Acids to be Used in Solid-Phase Glycopeptide Synthesis (Fmoc = Fluoren-9- ylmethoxycarbonyl)

ChemInform, 1991-01, Vol.22 (3), p.no-no

1991

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Enzymatic synthesis of the delicious peptide fragments in eutectic mixtures

Biologically active peptides and enzymatic approaches to their production

Optimization and kinetic studies of the enzymatic synthesis of Ac-Phe-Leu-NH2 in reversed micelles

Ethyl acetate modified AOT water-in-oil microemulsions for the α-chymotrypsin catalyzed synthesis of a model dipeptide derivative

Hydrolysis of N-protected amino acid allyl esters by enzymatic catalysis

Racemization free coupling of peptide segments : synthesis of an insect neuropeptide

Enzymatic peptide fragment condensation. Choice of reaction media for the synthesis of an insect neuropeptide derivative

Contribution of C-tail residues of potato carboxypeptidase inhibitor to the binding to carboxypeptidase A. A mutagenesis analysis

Ethyl acetate modified AOT water-in-oil microemulssions for the α-chymotrypsin catalyzed synthesis of a model dipeptide derivative

Arenesulphonyltriazolides as condensing reagents in solid phasepeptide synthesis

Anchoring of Fmoc-amino acids to hydroxymethyl resins

Arenesulphonyltriazolides as condensing reagents in solid phase peptide synthesis

Optimization and kinetic studies of the enzymatic synthesis of Ac-Phe-Leu-NH 2 in reversed micelles

Application of empirical design methodologies to the study of the influence of reaction conditions and N-α-protecting group structure on the enzymatic X-Phe-Leu-NH2 dipeptide synthesis in buffer/dimethylformamide solvent systems

New enzymatic approach to the synthesis of convenient aspartic acid intermediates in peptide chemistry. Synthesis of n-benzyloxycarbonyl-l-aspartic acid β-allyl ester

Application of empirical design methodologies to the study of the influence of reaction conditions and N-α-protecting group structure on the enzymatic X-Phe-Leu-NH2 dipeptide synthesis in buffer/dimethylformamide solvents systems

Application of empirical design methodologies to the study of the influence of reaction conditions and N-alpha-protecting group structure on the enzymatic X-Phe-Leu-NH(2) dipeptide synthesis in buffer/dimethylformamide solvents systems

New enzymatic approach to the synthesis of convenient aspartic acid intermediates in peptide chemistry: synthesis of N-benzoyloxycarbonyl-L-aspartic acid β-allyl ester

Application of empirical design methodologies to the study of the influence of reaction conditions and N ‐α‐protecting group structure on the enzymatic X‐Phe‐Leu‐NH 2 dipeptide synthesis in buffer/dimethylformamide solvents systems

Racemization free coupling of peptide segments

ChemInform Abstract: Arenesulfonyltriazolides as Condensing Reagents in Solid Phase Peptide Synthesis

Online coupled regional meteorology chemistry models in Europe: current status and prospects

A new NMVOC speciated inventory for a reactivity-based approach to support ozone control strategies in Spain

Improved method for the synthesis of o-glycosylated Fmoc amino acids to be used in solid-phase glycopeptide synthesis (Fmoc = fluoren-9-ylmethoxycarbonyl)

ChemInform Abstract: Improved Method for the Synthesis of O-Glycosylated Fmoc Amino Acids to be Used in Solid-Phase Glycopeptide Synthesis (Fmoc = Fluoren-9- ylmethoxycarbonyl)

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