Synthesis of short peptides using propargyloxycarbonyl amino acid chlorides as effective coupling reagents and polymer supported tetrathiomolybdate as an efficient deblocking agent are reported
At the time the present work was started, a new technique, the so-called FMOC/4-AMP method for rapid...
Amidation is the predominant reaction within the pharmaceutical setting, and it is attracting greate...
Peptide bond forming reactions are fundamental to the synthesis of peptides and peptidomimetics. Unf...
Synthesis of short peptides using propargyloxycarbonyl amino acid chlorides as effective coupling re...
Synthesis of short peptides using propargyloxycarbonyl amino acid chlorides as effective coupling re...
Propargyloxycarbonyl group is used as a protecting group for the hydroxyl groups of serine, threonin...
Coupling of Fmoc-amino acid chlorides mediated by activated commercial zinc dust for the synthesis o...
Propargyloxycarbonyl group is used as a protecting group for the hydroxyl groups of serine, threonin...
Propargyloxycarbonyl group is used as a protecting group for the hydroxyl groups of serine, threonin...
The combination of 1M silicon tetrachloride and 3M phenol serves as an efficient N(α)-t-butoxycarbon...
Oxytocin, a nonapeptide amide, was synthesized on a benzhydryl-resin using the Boc strategy. Benzyl ...
Peptide coupling with minimal protection is one of the desired methods for the synthesis of peptides...
The synthesis of peptides employing Fmoc-amino acid chlorides in presence of HOBt·DCHA salt in solut...
A high yield and rapid synthesis of enantiomerically pure N (alpha) -protected amino/peptide acid ar...
A high yield and rapid synthesis of enantiomerically pure N α -protected amino/peptide acid arylamid...
At the time the present work was started, a new technique, the so-called FMOC/4-AMP method for rapid...
Amidation is the predominant reaction within the pharmaceutical setting, and it is attracting greate...
Peptide bond forming reactions are fundamental to the synthesis of peptides and peptidomimetics. Unf...
Synthesis of short peptides using propargyloxycarbonyl amino acid chlorides as effective coupling re...
Synthesis of short peptides using propargyloxycarbonyl amino acid chlorides as effective coupling re...
Propargyloxycarbonyl group is used as a protecting group for the hydroxyl groups of serine, threonin...
Coupling of Fmoc-amino acid chlorides mediated by activated commercial zinc dust for the synthesis o...
Propargyloxycarbonyl group is used as a protecting group for the hydroxyl groups of serine, threonin...
Propargyloxycarbonyl group is used as a protecting group for the hydroxyl groups of serine, threonin...
The combination of 1M silicon tetrachloride and 3M phenol serves as an efficient N(α)-t-butoxycarbon...
Oxytocin, a nonapeptide amide, was synthesized on a benzhydryl-resin using the Boc strategy. Benzyl ...
Peptide coupling with minimal protection is one of the desired methods for the synthesis of peptides...
The synthesis of peptides employing Fmoc-amino acid chlorides in presence of HOBt·DCHA salt in solut...
A high yield and rapid synthesis of enantiomerically pure N (alpha) -protected amino/peptide acid ar...
A high yield and rapid synthesis of enantiomerically pure N α -protected amino/peptide acid arylamid...
At the time the present work was started, a new technique, the so-called FMOC/4-AMP method for rapid...
Amidation is the predominant reaction within the pharmaceutical setting, and it is attracting greate...
Peptide bond forming reactions are fundamental to the synthesis of peptides and peptidomimetics. Unf...
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