A new carboxy-protecting group for peptide synthesis and its direct conversion into an activated ester suitable for peptide formation: 4-(methylthio)phenyl and 4-(methylsulphonyl)phenyl esters

1968 ◽  
pp. 73b ◽  
Author(s):  
Brian J. Johnson ◽  
Paula M. Jacobs
Keyword(s):  
Peptide Synthesis ◽  
Direct Conversion ◽  
Protecting Group ◽  
Peptide Formation

o-Nitrobenzoyl group as a new amino protecting group for peptide synthesis and the synthesis of some anthranilyl peptides

Tetrahedron ◽  
1973 ◽  
Vol 29 (4) ◽  
pp. 625-628 ◽  
Author(s):  
A.K. Koul ◽  
J.M. Bachhawat ◽  
B. Prashad ◽  
N.S. Ramegowda ◽  
A.K. Mathur ◽  
...  
Keyword(s):  
Peptide Synthesis ◽  
Protecting Group

The 2-chloro-3-indenylmethyloxycarbonyl and benz[f]inden-3-ylmethyloxycarbonyl base-sensitive amino-protecting group. Application to an inverse Merrifield approach to peptide synthesis

1990 ◽  
Vol 55 (1) ◽  
pp. 251-259 ◽  
Author(s):  
Louis A. Carpino ◽  
Beri J. Cohen ◽  
Yao Zhong Lin ◽  
Kenton E. Stephens ◽  
Salvatore A. Triolo
Keyword(s):  
Peptide Synthesis ◽  
Protecting Group

ChemInform Abstract: New Strategies for an Efficient Removal of the 9-Fluorenylmethoxycarbonyl (Fmoc) Protecting Group in the Peptide Synthesis.

ChemInform ◽  
2010 ◽  
Vol 31 (16) ◽  
pp. no-no
Author(s):  
Antonella Leggio ◽  
Angelo Liguori ◽  
Anna Napoli ◽  
Carlo Siciliano ◽  
Giovanni Sindona
Keyword(s):  
Peptide Synthesis ◽  
Protecting Group ◽  
Efficient Removal ◽  
Fmoc Protecting Group ◽  
New Strategies
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