84000-04-4Relevant academic research and scientific papers
Fluorenylmethoxycarbonyl-N-methylamino acids synthesized in a flow tube-in-tube reactor with a liquid-liquid semipermeable membrane
Buba, Annette E.,Koch, Stefan,Kunz, Horst,Loewe, Holger
supporting information, p. 4509 - 4513 (2013/07/26)
Both steps of the N-methylation of 9-fluorenylmethoxycarbonyl (Fmoc) amino acids were carried out in a microstructured tube-in-tube reactor equipped with a semipermeable Teflon AF 2400 membrane as the inner tubing. In the first step, gaseous formaldehyde
Efficient synthesis of polyfunctionalised enantiopure diazepanone scaffolds
Monasson, Olivier,Ginisty, Maryon,Bertho, Gildas,Gravier-Pelletier, Christine,Le Merrer, Yves
, p. 8149 - 8152 (2008/03/13)
The synthesis of polyfunctionalised enantiopure 1,4-diazepan-3-one scaffolds from l-serine derivatives and azidoepoxides readily available from either l-ascorbic or d-isoascorbic acid, allowing access to various configurations at chiral centres, is descri
Synthesis of 9-Fluorenylmethyloxycarbonyl-Protected N-Alkyl Amino Acids by Reduction of Oxazolidinones
Freidinger, Roger M.,Hinkle, Jeffery S.,Perlow, Debra S.,Arison, Byron H.
, p. 77 - 81 (2007/10/02)
A new two-step synthesis of Fmoc-protected N-alkyl amino acids has been developed.The first step involves acid-catalyzed condensation of an Fmoc-protected amino acid with an aldehyde to form an oxazolidinone.This intermediate is then reduced with triethyl
