Acid-labile anchoring linkages for solid phase synthesis of C-terminal asparagine peptides using the Fmoc strategy

2009 ◽  
Vol 36 (2) ◽  
pp. 182-187 ◽  
Author(s):  
JUN SHAO ◽  
YOU-HE LI ◽  
WOLFGANG VOELTER
1992 ◽  
Vol 57 (8) ◽  
pp. 1707-1718
Author(s):  
Wolfgang Voelter ◽  
Gerhard Breipohl ◽  
Chryssa Tzougraki ◽  
Eveline Jungfleisch-Turgut

The solid phase synthesis of an amidated somatostatin analogue based on the principle of differentiated acidolysis is described. The acid labile and smoothly cleavable t-Bumeoc moiety (1% TFA/DCM) is used for temporary Nα-protection of D- and L-amino acids and [4-[[[9H-fluoren-9-yl-methoxycarbonyl]amino](4-methoxyphenyl)methyl]-2-methylphenoxy]acetic acid, attached to an aminomethylated polystyrene resin is used as acid sensitive linker of the solid carrier which releases the peptide in its amide form by treatment with TFA. Its preparation is described in detail.


Peptides 1994 ◽  
1995 ◽  
pp. 297-298
Author(s):  
S. G. Zakhariev ◽  
C. Guarnaccia ◽  
H.-G. Gattner ◽  
S. Pongor ◽  
D. Brandenburg

Peptides ◽  
1992 ◽  
pp. 601-602 ◽  
Author(s):  
Roger J. Bontems ◽  
Peter Hegyes ◽  
Susan L. Bontems ◽  
Fernando Albericio ◽  
George Barany

1996 ◽  
Vol 2 (5) ◽  
pp. 265-270 ◽  
Author(s):  
Michael F. Songster ◽  
Josef V�gner ◽  
George Barany

2006 ◽  
Vol 71 (18) ◽  
pp. 6734-6741 ◽  
Author(s):  
Mikkel Jessing ◽  
Malene Brandt ◽  
Knud J. Jensen ◽  
Jørn B. Christensen ◽  
Ulrik Boas

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