The introduction of benzyloxylcarbonyl (Z) group into amino acids is described at neutral pH using benzyloxylcarbonyl chloride and activated zinc powder. The reaction is simple, fast and clean. Thus the Z-amino acids are prepared in good yield and purity
Mentor: Dr. John GituaAmino acids are important biological compounds and useful chemical reagents in...
A new and efficient method for the synthesis ofNα-Fmoc-/Boc-/Z-β-amino acids using the two-step Arnd...
The coupling of urethane protected amine acid fluorides is accomplished in the presence of activated...
70-74The introduction of Nα-9-fluorenylmethyloxycarbonyl (Fmoc) and benzyloxycarbonyl (Z) groups in...
Synthesis of alkyl, aryl, heterocyclic, carbohydrate and amino acid carbamates is described. The pro...
Synthesis of alkyl, aryl, heterocyclic, carbohydrate and amino acid amides using activated zinc is d...
The pentafluorophenyl esters of Boc-/Z-amino acids are used for the preparation of the key intermedi...
A simple method for the synthesis of Z-/Boc-/Fmoc-protected β-amino acids by the Arndt-Eistert appro...
A range of N(α)-Fmoc-protected amino acids, including those that contain t-butyl moiety, have been ...
Amides of Z- and Boc protected amino acids have been prepared by using p-toluenesulphonyl chloride (...
A simple and scalable method for the preparation of N-Cbz protected amino acids is presented which u...
Coupling of Fmoc-amino acid chlorides mediated by activated commercial zinc dust for the synthesis o...
Synthesis of thiol esters from acyl chlorides and thiols in the presence of activated zinc is descri...
Department of Chemistry & Research Centre, Sarah Tucker College (Autonomous), affiliated to Manonma...
An unnatural amino acid, azalysine, was synthesized using several proposed procedures with the gener...
Mentor: Dr. John GituaAmino acids are important biological compounds and useful chemical reagents in...
A new and efficient method for the synthesis ofNα-Fmoc-/Boc-/Z-β-amino acids using the two-step Arnd...
The coupling of urethane protected amine acid fluorides is accomplished in the presence of activated...
70-74The introduction of Nα-9-fluorenylmethyloxycarbonyl (Fmoc) and benzyloxycarbonyl (Z) groups in...
Synthesis of alkyl, aryl, heterocyclic, carbohydrate and amino acid carbamates is described. The pro...
Synthesis of alkyl, aryl, heterocyclic, carbohydrate and amino acid amides using activated zinc is d...
The pentafluorophenyl esters of Boc-/Z-amino acids are used for the preparation of the key intermedi...
A simple method for the synthesis of Z-/Boc-/Fmoc-protected β-amino acids by the Arndt-Eistert appro...
A range of N(α)-Fmoc-protected amino acids, including those that contain t-butyl moiety, have been ...
Amides of Z- and Boc protected amino acids have been prepared by using p-toluenesulphonyl chloride (...
A simple and scalable method for the preparation of N-Cbz protected amino acids is presented which u...
Coupling of Fmoc-amino acid chlorides mediated by activated commercial zinc dust for the synthesis o...
Synthesis of thiol esters from acyl chlorides and thiols in the presence of activated zinc is descri...
Department of Chemistry & Research Centre, Sarah Tucker College (Autonomous), affiliated to Manonma...
An unnatural amino acid, azalysine, was synthesized using several proposed procedures with the gener...
Mentor: Dr. John GituaAmino acids are important biological compounds and useful chemical reagents in...
A new and efficient method for the synthesis ofNα-Fmoc-/Boc-/Z-β-amino acids using the two-step Arnd...
The coupling of urethane protected amine acid fluorides is accomplished in the presence of activated...