The Experts below are selected from a list of 318 Experts worldwide ranked by ideXlab platform
Hamid Reza Bijanzadeh - One of the best experts on this subject based on the ideXlab platform.
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synthesis of functionalized pseudopeptides through five component sequential ugi Nucleophilic Reaction of n substituted 2 alkynamides with hydrazides
ChemInform, 2013Co-Authors: Shokoofeh Maghari, Sorour Ramezanpour, Saeed Balalaie, Fatemeh Darvish, Frank Rominger, Hamid Reza BijanzadehAbstract:A novel approach for the synthesis of the title compounds containing hydrazones [e.g. (VI)] and vinyl hydrazide (XIV) groups is presented for a broad substrate scope.
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synthesis of functionalized pseudopeptides through five component sequential ugi Nucleophilic Reaction of n substituted 2 alkynamides with hydrazides
Journal of Organic Chemistry, 2013Co-Authors: Shokoofeh Maghari, Sorour Ramezanpour, Saeed Balalaie, Fatemeh Darvish, Frank Rominger, Hamid Reza BijanzadehAbstract:Five-component sequential Ugi/Nucleophilic addition Reaction of aromatic aldehydes, primary amines, propiolic acid, isocyanides, and hydrazides has been developed in order to access polyfunctional pseudopeptides. The Reaction may proceed through formation of N-substituted 2-alkynamides as intermediates. This process is found to be mild and operationally simple with broad substrate scope.
Shokoofeh Maghari - One of the best experts on this subject based on the ideXlab platform.
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synthesis of functionalized pseudopeptides through five component sequential ugi Nucleophilic Reaction of n substituted 2 alkynamides with hydrazides
ChemInform, 2013Co-Authors: Shokoofeh Maghari, Sorour Ramezanpour, Saeed Balalaie, Fatemeh Darvish, Frank Rominger, Hamid Reza BijanzadehAbstract:A novel approach for the synthesis of the title compounds containing hydrazones [e.g. (VI)] and vinyl hydrazide (XIV) groups is presented for a broad substrate scope.
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synthesis of functionalized pseudopeptides through five component sequential ugi Nucleophilic Reaction of n substituted 2 alkynamides with hydrazides
Journal of Organic Chemistry, 2013Co-Authors: Shokoofeh Maghari, Sorour Ramezanpour, Saeed Balalaie, Fatemeh Darvish, Frank Rominger, Hamid Reza BijanzadehAbstract:Five-component sequential Ugi/Nucleophilic addition Reaction of aromatic aldehydes, primary amines, propiolic acid, isocyanides, and hydrazides has been developed in order to access polyfunctional pseudopeptides. The Reaction may proceed through formation of N-substituted 2-alkynamides as intermediates. This process is found to be mild and operationally simple with broad substrate scope.
Saeed Balalaie - One of the best experts on this subject based on the ideXlab platform.
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synthesis of functionalized pseudopeptides through five component sequential ugi Nucleophilic Reaction of n substituted 2 alkynamides with hydrazides
ChemInform, 2013Co-Authors: Shokoofeh Maghari, Sorour Ramezanpour, Saeed Balalaie, Fatemeh Darvish, Frank Rominger, Hamid Reza BijanzadehAbstract:A novel approach for the synthesis of the title compounds containing hydrazones [e.g. (VI)] and vinyl hydrazide (XIV) groups is presented for a broad substrate scope.
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synthesis of functionalized pseudopeptides through five component sequential ugi Nucleophilic Reaction of n substituted 2 alkynamides with hydrazides
Journal of Organic Chemistry, 2013Co-Authors: Shokoofeh Maghari, Sorour Ramezanpour, Saeed Balalaie, Fatemeh Darvish, Frank Rominger, Hamid Reza BijanzadehAbstract:Five-component sequential Ugi/Nucleophilic addition Reaction of aromatic aldehydes, primary amines, propiolic acid, isocyanides, and hydrazides has been developed in order to access polyfunctional pseudopeptides. The Reaction may proceed through formation of N-substituted 2-alkynamides as intermediates. This process is found to be mild and operationally simple with broad substrate scope.
Fatemeh Darvish - One of the best experts on this subject based on the ideXlab platform.
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synthesis of functionalized pseudopeptides through five component sequential ugi Nucleophilic Reaction of n substituted 2 alkynamides with hydrazides
ChemInform, 2013Co-Authors: Shokoofeh Maghari, Sorour Ramezanpour, Saeed Balalaie, Fatemeh Darvish, Frank Rominger, Hamid Reza BijanzadehAbstract:A novel approach for the synthesis of the title compounds containing hydrazones [e.g. (VI)] and vinyl hydrazide (XIV) groups is presented for a broad substrate scope.
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synthesis of functionalized pseudopeptides through five component sequential ugi Nucleophilic Reaction of n substituted 2 alkynamides with hydrazides
Journal of Organic Chemistry, 2013Co-Authors: Shokoofeh Maghari, Sorour Ramezanpour, Saeed Balalaie, Fatemeh Darvish, Frank Rominger, Hamid Reza BijanzadehAbstract:Five-component sequential Ugi/Nucleophilic addition Reaction of aromatic aldehydes, primary amines, propiolic acid, isocyanides, and hydrazides has been developed in order to access polyfunctional pseudopeptides. The Reaction may proceed through formation of N-substituted 2-alkynamides as intermediates. This process is found to be mild and operationally simple with broad substrate scope.
Frank Rominger - One of the best experts on this subject based on the ideXlab platform.
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synthesis of functionalized pseudopeptides through five component sequential ugi Nucleophilic Reaction of n substituted 2 alkynamides with hydrazides
ChemInform, 2013Co-Authors: Shokoofeh Maghari, Sorour Ramezanpour, Saeed Balalaie, Fatemeh Darvish, Frank Rominger, Hamid Reza BijanzadehAbstract:A novel approach for the synthesis of the title compounds containing hydrazones [e.g. (VI)] and vinyl hydrazide (XIV) groups is presented for a broad substrate scope.
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synthesis of functionalized pseudopeptides through five component sequential ugi Nucleophilic Reaction of n substituted 2 alkynamides with hydrazides
Journal of Organic Chemistry, 2013Co-Authors: Shokoofeh Maghari, Sorour Ramezanpour, Saeed Balalaie, Fatemeh Darvish, Frank Rominger, Hamid Reza BijanzadehAbstract:Five-component sequential Ugi/Nucleophilic addition Reaction of aromatic aldehydes, primary amines, propiolic acid, isocyanides, and hydrazides has been developed in order to access polyfunctional pseudopeptides. The Reaction may proceed through formation of N-substituted 2-alkynamides as intermediates. This process is found to be mild and operationally simple with broad substrate scope.