71989-13-4Relevant articles and documents
AN EFFICIENT METHOD FOR RACEMIZATION FREE ATTACHMENT OF 9-FLUORENYLMETHYLOXYCARBONYL-AMINO ACIDS TO PEPTIDE SYNTHESIS SUPPORTS
Bernatowicz, Michael S.,Kearney, Thomas,Neves, Richard S.,Koester, Hubert
, p. 4341 - 4344 (1989)
An efficient, general, and racemization free method of covalently attaching N α-Fmoc protected amino acids to solid supports for peptide synthesis is described.The process involves the preparation of 2,4-dichlorophenyl-N α-Fmoc- aminoacyl-4-oxymethyl-phen
Active Esters of 9-Fluorenylmethyloxycarbonyl Amino Acids and Their Application in the Stepwise Lengthening of a Peptide Chain
Bodanszky, Agnes,Bodanszky, Miklos,Chandramouli, Nagarajan,Kwei, Joseph Z.,Martinez, Jean,Tolle, John C.
, p. 72 - 76 (2007/10/02)
Preparation and properties of p-nitrophenyl esters of several 9-fluorenylmethyloxycarbonyl (Fmoc) amino acids are described.The Fmoc derivatives of the hindered amino acids valine and isoleucine were converted to the more reactive o-nitrophenyl esters whi