910-919Highly active and shelf stable pentafluoro phenol derived Fmoc-peptidyl carbamates have been synthesized from corresponding Fmoc-peptidyl isocyanates. The utility of pentafluorophenyl carbamate intermediates has been demonstrated by the synthesis of tri, penta and hexapeptidyl ureas which are obtained in good yields. All the synthesised compounds have been characterized by ¹H NMR, ¹³C NMR and mass spectroscopy. The coupling reaction using pentafluorophenyl carbamates to insert urea bond between α amino acids is fast, clean and high yielding
In the search for new drug compounds, the current focus has been shifted to a class of compounds cal...
The Curtius rearrangement of Fmoc-amino acid azides 1 was carried out in toluene by refluxing the so...
A simple protocol for the synthesis of linear peptidylcarbamates employing Fmoc-β-aminoalkoxy carbo...
Highly active and shelf stable pentafluoro phenol derived Fmoc-peptidyl carbamates have been synthes...
The one-pot synthesis of pentafluorophenyl-(tert-butoxycarbonylamino)methyl carbamates starting from...
A rapid and efficient method for the synthesis of peptidyl ureas employing O-pentafluoro phenyl-(9-f...
An efficient synthesis of p-nitrophenyl-(9-fluorenylmethoxy carbonylamino) methyl carbamates using i...
69-76 An efficient method for the synthesis of O-succinimidyl (9H-fluorene-9-yl methoxycarbonylamine...
An efficient method for the synthesis of O-succinimidyl (9H-fluorene-9-yl methoxycarbonylamine) pept...
An efficient synthesis of 2,4,5-trichlorophenyl-(9H-fluoren-9- ylmethoxycarbonylamino)methylcarbamat...
A convenient and efficient method for the synthesis of dipeptidyl ureas and urea acids employing O-s...
N-Fmoc-Aminoalkoxy pentafluorophenyl carbonates have been synthesized through the reaction of N-Fmoc...
(Chemical Equation Presented) The Nα-Fmoc-peptide isocyanates 3a-q, 4a-c, and 5a-c were prepared by...
Carbamates Fmoc-NHCHRNHCO2C6H4NO2-p (Fmoc is 9-fluorenylmethoxycarbonyl, R is an amino acid side ...
Application of the Lossen rearrangement to the synthesis of N-urethane protected α-peptidyl ureas an...
In the search for new drug compounds, the current focus has been shifted to a class of compounds cal...
The Curtius rearrangement of Fmoc-amino acid azides 1 was carried out in toluene by refluxing the so...
A simple protocol for the synthesis of linear peptidylcarbamates employing Fmoc-β-aminoalkoxy carbo...
Highly active and shelf stable pentafluoro phenol derived Fmoc-peptidyl carbamates have been synthes...
The one-pot synthesis of pentafluorophenyl-(tert-butoxycarbonylamino)methyl carbamates starting from...
A rapid and efficient method for the synthesis of peptidyl ureas employing O-pentafluoro phenyl-(9-f...
An efficient synthesis of p-nitrophenyl-(9-fluorenylmethoxy carbonylamino) methyl carbamates using i...
69-76 An efficient method for the synthesis of O-succinimidyl (9H-fluorene-9-yl methoxycarbonylamine...
An efficient method for the synthesis of O-succinimidyl (9H-fluorene-9-yl methoxycarbonylamine) pept...
An efficient synthesis of 2,4,5-trichlorophenyl-(9H-fluoren-9- ylmethoxycarbonylamino)methylcarbamat...
A convenient and efficient method for the synthesis of dipeptidyl ureas and urea acids employing O-s...
N-Fmoc-Aminoalkoxy pentafluorophenyl carbonates have been synthesized through the reaction of N-Fmoc...
(Chemical Equation Presented) The Nα-Fmoc-peptide isocyanates 3a-q, 4a-c, and 5a-c were prepared by...
Carbamates Fmoc-NHCHRNHCO2C6H4NO2-p (Fmoc is 9-fluorenylmethoxycarbonyl, R is an amino acid side ...
Application of the Lossen rearrangement to the synthesis of N-urethane protected α-peptidyl ureas an...
In the search for new drug compounds, the current focus has been shifted to a class of compounds cal...
The Curtius rearrangement of Fmoc-amino acid azides 1 was carried out in toluene by refluxing the so...
A simple protocol for the synthesis of linear peptidylcarbamates employing Fmoc-β-aminoalkoxy carbo...