Amino Acids

1. N-Fmoc-a-sulfo-b-alanine: a versatile building block for the water solubilisation of chromophores and fluorophores by solid-phase strategy
   25.01.2017

   142
   Anthony Romieu, Thomas Bruckdorfer, Guillaume Clavé, Virgile Grandclaude, Cédrik Massif and Pierre-Yves Renard Org. Biomol. Chem.2011; 9:5337. DOI: 10.1039/c1ob05730h Abstract: An easy and efficient solid-phase synthesis strategy to obtain rapidly water-soluble ...
2. Shorter Arginine homologues to stabilize peptides towards tryptic digestion
   25.01.2017

   117
   Petra Henklein, Thomas Bruckdorfer Chemistry Today 2008; 26(6):12-15. Abstract: Trypsin digests peptides at the position of arginine. Because shorter homologues of arginine with appropriate protecting groups for conventional Fmoc/tBu peptide synthesis are now available, three model peptides ...
3. Synthesis of side-chain to side-chain cyclic peptides and oligolysine cores suitable for the solid-phase assembly of MAPs and TASPs.
   25.01.2017

   161
   Aletras A; Barlos K; Gatos D; Koutsogianni S; Mamos P International Journal of Peptide and Protein Research 1995; 45(5): 488-96. Abstract: The Nε-Mtt function of Nα-9-Fluorenylmethoxycarbonyl-Nε-4-methyltrityl-lysine, [Fmoc-Lys(Mtt)-OH] can be quantitatively removed ...
4. Application of the Trt and Fmoc groups for the protection of polyfunctional α-amino acids.
   25.01.2017

   126
   Barlos, Kleomenis; Mamos, Petros; Papaioannou, Dionysios; Patrianakou, Stella; Sanida, Chariklia; Schaefer, Wolfram. Liebigs Annalen der Chemie1987; 12:1025-30. Abstract: Ditrityl amino acids Trt-Lys(Trt)-OH (Trt = CPh3), Trt-Orn(Trt)-OH, Trt-Ser(Trt)-OH, and Trt-Hse(Trt)-OH were prepared ...