Orthogonally protected, carboxy-activated L-homoisoserine, 2-methyl-L-homoisoserine, and homoisocysteine derivatives. New building blocks for peptide and depsipeptide modification

Monatshefte fur Chemie

Volumn 136, Issue 5, 2005, Pages 763-776

  Burger, Klaus ^a   Radics, Gabor ^a   Hennig, Lothar ^a   Böttcher, Christoph ^a   Spengler, Jan ^b   Albericio, Fernando ^b  

^a UNIVERSITY OF LEIPZIG   (Germany)

^b INSTITUTE FOR RESEARCH IN BIOMEDICINE   (Spain)

Author keywords

Hydroxy acids; Mercapto acids; Amino acids; Arndt Eistert reaction; Azapeptides; Citramalic acid; Curtius rearrangement; Depsipeptide modification; Hexafluoroacetone; Malic acid; Peptide modification; Thiomalic acid; Wolff rearrangement

Indexed keywords

4 AMINOBUTYRIC ACID; CYSTEINE DERIVATIVE; DEPSIPEPTIDE; MALIC ACID; MALIC ACID DERIVATIVE; PEPTIDE; PEPTIDE DERIVATIVE; SERINE DERIVATIVE; THIOMALIC ACID;

ARTICLE; CATALYSIS; CHEMICAL MODIFICATION; DECOMPOSITION; DERIVATIZATION; DRUG SYNTHESIS; HEATING; ROOM TEMPERATURE;

EID: 18544382656     PISSN: 00269247     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00706-005-0291-1     Document Type: Article

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