Application of acetamidomethyl and 9‐fluorenylmethyl groups for efficient side protection of penicillamine in solid‐phase peptide synthesis

International Journal of Peptide and Protein Research

Volumn 35, Issue 5, 1990, Pages 434-440

  GARCÍA‐ECHEVERRÍA, CARLOS ^a   MOLINS, M ANTONIA ^a   ALBERICIO, FERNANDO ^a   PONS, MIQUEL ^a   GIRALT, ERNEST ^a  

^a UNIVERSITY OF BARCELONA   (Spain)

Author keywords

9 fluorenylmethyl; acetamidomethyl; disulfide bridge; penicillamine; solid phase peptide synthesis; thiol protection

Indexed keywords

FLUORENE DERIVATIVE; PENICILLAMINE DERIVATIVE; THIOL GROUP;

ARTICLE; CHEMICAL PROTECTION; PEPTIDE SYNTHESIS; SOLID PHASE CHEMISTRY;

AMINO ACID SEQUENCE; MOLECULAR SEQUENCE DATA; MOLECULAR STRUCTURE; PENICILLAMINE; PEPTIDE FRAGMENTS; SUPPORT, NON-U.S. GOV'T;

EID: 0025324009     PISSN: 03678377     EISSN: 13993011     Source Type: Journal    
DOI: 10.1111/j.1399-3011.1990.tb00070.x     Document Type: Article

References (31)

1. Design of a new class of superpotent cyclic .alpha.-melanotropins based on quenched dynamic simulations
2. Peptide synthesis. Part 6. Protection of the sulphydryl group of cysteine in solid-phase synthesis using N ?-fluorenylmethoxycarbonylamino acids. Linear oxytocin derivatives
3. Structure determination of a tetrasaccharide: transient nuclear Overhauser effects in the rotating frame