The synthesis, optical resolution, determination of absolute configuration and conformational preference, and spectroscopic characteristics of terminally protected (blocked) derivatives and short peptides of 2-amino-1,2,3,6-tetrahydro-6-oxocyclopenta[c]fluorene-2-carboxylic acid (FlAib), a novel, rigid, chiral, cyclized Ca,a-disubstituted glycine are described.

2-Amino-1,2,3,6-tetrahydro-6-oxocyclopenta[c]fluorene-2-carboxylic Acid (FlAib), a Completely Rigidified, Fluoren-9-one-Basedα-Amino Acid

TOFFOLETTI, ANTONIO;FORMAGGIO, FERNANDO;TONIOLO, CLAUDIO
2012

Abstract

The synthesis, optical resolution, determination of absolute configuration and conformational preference, and spectroscopic characteristics of terminally protected (blocked) derivatives and short peptides of 2-amino-1,2,3,6-tetrahydro-6-oxocyclopenta[c]fluorene-2-carboxylic acid (FlAib), a novel, rigid, chiral, cyclized Ca,a-disubstituted glycine are described.
2012
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11577/2574369
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