736127-53-0Relevant academic research and scientific papers
Helical folding of α/β-peptides containing β-amino acids with an eight-membered ring constraint
Lee, Woohyung,Kwon, Sunmi,Kang, Philjae,Guzei, Ilia A.,Choi, Soo Hyuk
supporting information, p. 2641 - 2644 (2014/05/06)
αβα-Tripeptide that contains a cyclic β-amino acid with an eight-membered ring, a cis-2-aminocyclooct-5-enecarboxylic acid (cis-ACOE) or a cis-2-aminocyclooctanecarboxylic acid (cis-ACOC) displayed an 11/9-helical turn in the crystal state. The related α/β-peptide oligomers were shown to adopt 11/9-helical conformations in solution. This journal is the Partner Organisations 2014.
Synthesis of mono- and dihydroxy-substituted 2-aminocyclooctanecarboxylic acid enantiomers
Palko, Marta,Benedek, Gabriella,Forro, Enik,Weber, Edit,Haenninen, Mikko,Sillanpaeae, Reijo,Fueloep, Ferenc
experimental part, p. 957 - 961 (2010/08/06)
(1R,2S,6R)-2-Amino-6-hydroxycyclooctanecarboxylic acid (-)-10 was synthesized from (1R,2S)-2-aminocyclooct-5-enecarboxylic acid (+)-2 via an iodolactone intermediate, while (1R,2S,3R,4S)-2-amino-5,6- dihydroxycyclooctanecarboxylic acid (-)-12 was prepared
Advanced procedure for the enzymatic ring opening of unsaturated alicyclic β-lactams
Forro, Eniko,Fueloep, Ferenc
, p. 2875 - 2880 (2007/10/03)
Enantiopure β-amino acids 1a-4a and β-lactams 1b-4b were prepared simultaneously through the lipolase-catalysed enantioselective ring opening of unsaturated racemic β-lactams (±)-1-(±)-4. High enantioselectivities (E>200) were observed when the reactions
