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Structural Insight on the Activity of Type 1 Angiotensin II Peptide Antagonists Using MD Simulations

The journal of physical chemistry. B, 2008-10, Vol.112 (43), p.13620-13628

2008

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Straightforward, racemization-free synthesis of peptides with fairly to very bulky di- and trisubstituted glycines

Tetrahedron, 2009-11, Vol.65 (45), p.9165-9179

2009

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2-Naphthalenesulfonyl as a Tosyl Substitute for Protection of Amino Functions. Cyclic Voltammetry Studies on Model Sulfonamides and Their Preparative Cleavage by Reduction

Journal of organic chemistry, 1999-09, Vol.64 (19), p.7135-7139

1999

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Molecular Dynamics Simulations of Angiotensin II in Aqueous and Dimethyl Sulfoxide Environments

The journal of physical chemistry. B, 2005-09, Vol.109 (37), p.17743-17751

2005

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Enhancing Reductive Cleavage of Aromatic Carboxamides

Organic letters, 2001-06, Vol.3 (13), p.2021-2023

2001

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Effect of temperature on the acidolysis of N-acyl-N,α,α-trialkyl glycine amides as related to the nature of substituents

Journal of peptide science, 2006-03, Vol.12 (3), p.239-242

2006

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Kinetic and mechanistic investigation of the selective acidolysis of the C-terminal amide bond of N-acyl-N,α,α-trialkyl glycine amides

Journal of peptide science, 2005-08, Vol.11 (8), p.472-480

2005

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Kinetic investigation of the effect of the amino acid side chains in the selective acidolysis of N-acyl-N,α,α-trialkyl glycine amides

Journal of peptide science, 2005-10, Vol.11 (10), p.627-632

2005

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Differences in Backbone Structure between Angiotensin II Agonists and Type I Antagonists

Journal of medicinal chemistry, 1995-11, Vol.38 (23), p.4660-4669

1995

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Synthesis of N-acyl-N,alpha,alpha-trialkyl and N-acyl-alpha,alpha-dialkyl glycines by selective cleavage of Ugi-Passerini adducts. Qualitative assessment of the effect of substituents on the path and yield of reaction

Organic & biomolecular chemistry, 2003-11, Vol.1 (21), p.3804-3810

2003

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Synthesis and kinetic investigation of the selective acidolysis of para-substituted N-benzyl- or N-phenyl- N-phenylacetyl-α,α-dialkylglycine cyclohexylamides

Tetrahedron, 2006-08, Vol.62 (34), p.8184-8198

2006

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Development of a temporary marker for peptidesElectronic supplementary information (ESI) available: IR, UV, 1H NMR and 13C NMR spectra of compounds 2a–i, 3b–h, 4b–h, 5, 6c and h, 7h, 8–12, 13c and h, and 14. See http://www.rsc.org/suppdata/ob/b2/b212470j

Organic & biomolecular chemistry, 2003-04, Vol.1 (9), p.1480-1485

2003

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An improved approach for the synthesis of α,α-dialkyl glycine derivatives by the Ugi–Passerini reactionElectronic supplementary information (ESI) available: spectroscopic data for compounds 1-5. See http://www.rsc.org/suppdata/ob/b2/b212473b

Organic & biomolecular chemistry, 2003-04, Vol.1 (9), p.1475-1479

2003

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Mild Reductive Cleavage of Tryptophan and Histidine Side-Chain Protecting Groups

European journal of organic chemistry, 2001-05, Vol.2001 (10), p.1967-1970

2001

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Selective cathodic cleavage of unsymmetrical imidodicarbonates, acylcarbamates and diacylamides

Journal of the Chemical Society, Perkin Transactions 2, 1993 (3), p.495

1993

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Synthesis and cathodic cleavage of a set of substituted benzenesulfonamides including the corresponding tert-butyl sulfonylcarbamates: pK a of sulfonamides

Journal of the Chemical Society, Perkin Transactions 1, 1995 (16), p.2025

1995

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Structural versatility of peptides from C α,α -disubstituted glycines. Preferred conformation of the C α,α -dibenzylglycine residue

J. Chem. Soc., Perkin Trans. 2, 1990 (8), p.1481-1487

1990

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Synthesis of Non-Natural Amino Acids from N-(p-Tolylsulfonyl)-α,β-didehydroamino Acid Derivatives

European journal of organic chemistry, 2003-07, Vol.2003 (14), p.2635-2644

2003

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The cathodic cleavage of the 4-nitrobenzyloxycarbonyl group from amine derivatives in aprotic conditions

Journal of the Chemical Society, Perkin Transactions 2, 1988 (3), p.409

1988

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The anodic oxidation of 2-(4-nitrophenylthio)ethyl esters in acetonitrile

Journal of the Chemical Society, Perkin Transactions 2, 1989 (11), p.1707

1989

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Michael addition of thiols, carbon nucleophiles and amines to dehydroamino acid and dehydropeptide derivativesElectronic supplementary information (ESI) available: experimental data for compounds 1–15. See http://www.rsc.org/suppdata/p1/b1/b106487h

Perkin 1 : an international journal of organic and bio-organic chemistry, 2001-11 (23), p.3167-3173

2001

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Reductive cleavage of N-substituted aromatic amides as tert-butyl acylcarbamatesElectronic supplementary information (ESI) available: reductive cleavage of N-substituted aromatic amides as tert-butyl acylcarbamates. See http://www.rsc.org/suppdata/p1/b1/b107330n

Perkin 1 : an international journal of organic and bio-organic chemistry, 2002-12 (1), p.97-101

2002

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Parametrization of Synthetic Amino Acids

The journal of physical chemistry. B, 2003-12, Vol.107 (51), p.14556-14562

2003

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Effect of temperature on the acidolysis ofN-acyl-N,α,α-trialkyl glycine amides as related to the nature of substituents

Journal of peptide science, 2006-03, Vol.12 (3), p.239-242

2006

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Synthesis and Conformational Investigation of Tetrapeptide Analogues of the Fragment B23-B26 of Insulin

ChemInform, 2004-12, Vol.35 (52), p.no-no

2004

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Structural Insight on the Activity of Type 1 Angiotensin II Peptide Antagonists Using MD Simulations

Straightforward, racemization-free synthesis of peptides with fairly to very bulky di- and trisubstituted glycines

2-Naphthalenesulfonyl as a Tosyl Substitute for Protection of Amino Functions. Cyclic Voltammetry Studies on Model Sulfonamides and Their Preparative Cleavage by Reduction

Molecular Dynamics Simulations of Angiotensin II in Aqueous and Dimethyl Sulfoxide Environments

Enhancing Reductive Cleavage of Aromatic Carboxamides

Effect of temperature on the acidolysis of N-acyl-N,α,α-trialkyl glycine amides as related to the nature of substituents

Kinetic and mechanistic investigation of the selective acidolysis of the C-terminal amide bond of N-acyl-N,α,α-trialkyl glycine amides

Kinetic investigation of the effect of the amino acid side chains in the selective acidolysis of N-acyl-N,α,α-trialkyl glycine amides

Differences in Backbone Structure between Angiotensin II Agonists and Type I Antagonists

Synthesis of N-acyl-N,alpha,alpha-trialkyl and N-acyl-alpha,alpha-dialkyl glycines by selective cleavage of Ugi-Passerini adducts. Qualitative assessment of the effect of substituents on the path and yield of reaction

Synthesis and kinetic investigation of the selective acidolysis of para-substituted N-benzyl- or N-phenyl- N-phenylacetyl-α,α-dialkylglycine cyclohexylamides

Development of a temporary marker for peptidesElectronic supplementary information (ESI) available: IR, UV, 1H NMR and 13C NMR spectra of compounds 2a–i, 3b–h, 4b–h, 5, 6c and h, 7h, 8–12, 13c and h, and 14. See http://www.rsc.org/suppdata/ob/b2/b212470j

An improved approach for the synthesis of α,α-dialkyl glycine derivatives by the Ugi–Passerini reactionElectronic supplementary information (ESI) available: spectroscopic data for compounds 1-5. See http://www.rsc.org/suppdata/ob/b2/b212473b

Mild Reductive Cleavage of Tryptophan and Histidine Side-Chain Protecting Groups

Selective cathodic cleavage of unsymmetrical imidodicarbonates, acylcarbamates and diacylamides

Synthesis and cathodic cleavage of a set of substituted benzenesulfonamides including the corresponding tert-butyl sulfonylcarbamates: pK a of sulfonamides

Structural versatility of peptides from C α,α -disubstituted glycines. Preferred conformation of the C α,α -dibenzylglycine residue

Synthesis of Non-Natural Amino Acids from N-(p-Tolylsulfonyl)-α,β-didehydroamino Acid Derivatives

The cathodic cleavage of the 4-nitrobenzyloxycarbonyl group from amine derivatives in aprotic conditions

The anodic oxidation of 2-(4-nitrophenylthio)ethyl esters in acetonitrile

Michael addition of thiols, carbon nucleophiles and amines to dehydroamino acid and dehydropeptide derivativesElectronic supplementary information (ESI) available: experimental data for compounds 1–15. See http://www.rsc.org/suppdata/p1/b1/b106487h

Reductive cleavage of N-substituted aromatic amides as tert-butyl acylcarbamatesElectronic supplementary information (ESI) available: reductive cleavage of N-substituted aromatic amides as tert-butyl acylcarbamates. See http://www.rsc.org/suppdata/p1/b1/b107330n

Parametrization of Synthetic Amino Acids

Effect of temperature on the acidolysis ofN-acyl-N,α,α-trialkyl glycine amides as related to the nature of substituents

Synthesis and Conformational Investigation of Tetrapeptide Analogues of the Fragment B23-B26 of Insulin

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