Synthetically useful Nb-Fmoc amino alkyl isonitriles are prepared conveniently from Nb-Fmoc amino alkyl thioformamides via a cyanogen bromide mediated dehydrosulfurization. The reac-tion is fast, clean, and yields are good
Sulfonylureas are employed in a variety of applications including use as drugs to treat type II diab...
Nitriles are valuable intermediates in organic synthesis not only because they serve as the appropri...
An in-water dehydration of N-formamides to afford isocyanides using micellar conditions at room temp...
Synthetically useful Nβ-Fmoc amino alkyl isonitriles are prepared conveniently from Nβ-Fmoc amino ...
An optimized ultrasound promoted procedure for the synthesis of the thioformamides is developed and ...
Chiral amino acid-derived formamides represent one of the most versatile components in multicomponen...
A unified approach to access Nβ-protected amino alkyl isothiocyanates using Nβ-protected amino alkyl...
Enantiopure Nß-Fmoc-amino alkyl isonitriles and amino acid esters have been employed as building blo...
Sulfonimidamides are intriguing new motifs for medicinal and agrochemistry, and provide attractive b...
An efficient isocyanide-based synthesis of S-thiocarbamates was discovered and thoroughly investigat...
Enantiopure N β-Fmoc-amino alkyl isonitriles and amino acid esters have been employed as building b...
Synthesis protocols to convert N-formamides into isocyanides using three different dehydration reage...
Thioamides are important biophysical probes of peptide folding but are prone to α-C epimerization du...
An efficient synthesis of Nα-protected amino nitriles from Nα-protected amino acid amides employing ...
Recently we reported the use of a sequence of alkylation and dehydration methodologies to obtain fro...
Sulfonylureas are employed in a variety of applications including use as drugs to treat type II diab...
Nitriles are valuable intermediates in organic synthesis not only because they serve as the appropri...
An in-water dehydration of N-formamides to afford isocyanides using micellar conditions at room temp...
Synthetically useful Nβ-Fmoc amino alkyl isonitriles are prepared conveniently from Nβ-Fmoc amino ...
An optimized ultrasound promoted procedure for the synthesis of the thioformamides is developed and ...
Chiral amino acid-derived formamides represent one of the most versatile components in multicomponen...
A unified approach to access Nβ-protected amino alkyl isothiocyanates using Nβ-protected amino alkyl...
Enantiopure Nß-Fmoc-amino alkyl isonitriles and amino acid esters have been employed as building blo...
Sulfonimidamides are intriguing new motifs for medicinal and agrochemistry, and provide attractive b...
An efficient isocyanide-based synthesis of S-thiocarbamates was discovered and thoroughly investigat...
Enantiopure N β-Fmoc-amino alkyl isonitriles and amino acid esters have been employed as building b...
Synthesis protocols to convert N-formamides into isocyanides using three different dehydration reage...
Thioamides are important biophysical probes of peptide folding but are prone to α-C epimerization du...
An efficient synthesis of Nα-protected amino nitriles from Nα-protected amino acid amides employing ...
Recently we reported the use of a sequence of alkylation and dehydration methodologies to obtain fro...
Sulfonylureas are employed in a variety of applications including use as drugs to treat type II diab...
Nitriles are valuable intermediates in organic synthesis not only because they serve as the appropri...
An in-water dehydration of N-formamides to afford isocyanides using micellar conditions at room temp...
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