A simple and scalable method for the preparation of N-Cbz protected amino acids is presented which uses a mixture of aqueous sodium carbonate and sodium bicarbonate to maintain the appropriate pH during the addition of benzyl chloroformate. The method has been extended to other N-protections and is amenable to large scale preparation of an intermediate toward Zofenopril, an ACE inhibitor. © 2011 Elsevier Ltd. All rights reserved.Ashok D. Pehere and Andrew D. Abellhttp://www.elsevier.com/wps/find/homepage.cws_hom
A fast and simple one-pot synthesis of carbamoyl azides of \u3b1-N-protected amino acids is reported...
A synthetic strategy to prepare o-NBS protected Fmoc-amino acids under mild conditions, in a rapid a...
Coupling of Fmoc-amino acid chlorides mediated by activated commercial zinc dust for the synthesis o...
The introduction of benzyloxylcarbonyl (Z) group into amino acids is described at neutral pH using b...
A range of N(α)-Fmoc-protected amino acids, including those that contain t-butyl moiety, have been ...
Racemization free synthesis of Nα-protected amino hydroxamic acids from Nα-protected amino acids emp...
A novel route has been developed for the solid-phase synthesis of N-carboxyalkyl unnatural amino aci...
International audienceAmino acid N-carboxyanhydrides (NCA), convenient monomer for polypeptide synth...
An efficient and stereospecific homologation of urethane-protected α-amino acids to β-amino acids ...
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extr...
Synthesis of alkyl, aryl, heterocyclic, carbohydrate and amino acid carbamates is described. The pro...
A simple method for the synthesis of Z-/Boc-/Fmoc-protected β-amino acids by the Arndt-Eistert appro...
A mild and simple procedure for the esterification of N-protected amino acids is described involving...
A new and efficient method for the synthesis of N-alpha-Fmoc-/Boc-/Z-beta-amino acids using the two-...
An efficient method for the activation of Fmoc/Boc/Cbz-protected amino acids using Boc2O and the red...
A fast and simple one-pot synthesis of carbamoyl azides of \u3b1-N-protected amino acids is reported...
A synthetic strategy to prepare o-NBS protected Fmoc-amino acids under mild conditions, in a rapid a...
Coupling of Fmoc-amino acid chlorides mediated by activated commercial zinc dust for the synthesis o...
The introduction of benzyloxylcarbonyl (Z) group into amino acids is described at neutral pH using b...
A range of N(α)-Fmoc-protected amino acids, including those that contain t-butyl moiety, have been ...
Racemization free synthesis of Nα-protected amino hydroxamic acids from Nα-protected amino acids emp...
A novel route has been developed for the solid-phase synthesis of N-carboxyalkyl unnatural amino aci...
International audienceAmino acid N-carboxyanhydrides (NCA), convenient monomer for polypeptide synth...
An efficient and stereospecific homologation of urethane-protected α-amino acids to β-amino acids ...
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extr...
Synthesis of alkyl, aryl, heterocyclic, carbohydrate and amino acid carbamates is described. The pro...
A simple method for the synthesis of Z-/Boc-/Fmoc-protected β-amino acids by the Arndt-Eistert appro...
A mild and simple procedure for the esterification of N-protected amino acids is described involving...
A new and efficient method for the synthesis of N-alpha-Fmoc-/Boc-/Z-beta-amino acids using the two-...
An efficient method for the activation of Fmoc/Boc/Cbz-protected amino acids using Boc2O and the red...
A fast and simple one-pot synthesis of carbamoyl azides of \u3b1-N-protected amino acids is reported...
A synthetic strategy to prepare o-NBS protected Fmoc-amino acids under mild conditions, in a rapid a...
Coupling of Fmoc-amino acid chlorides mediated by activated commercial zinc dust for the synthesis o...