ChemInform Abstract: REDUCTION OF METHIONINE SULFOXIDE IN PEPTIDE SYNTHESIS BY USE OF 2-MERCAPTOPYRIDINE IN LIQUID HYDROGEN FLUORIDE

1982 ◽  
Vol 13 (44) ◽  
Author(s):  
D. YAMASHIRO
1981 ◽  
Vol 46 (1) ◽  
pp. 286-299 ◽  
Author(s):  
František Brtník ◽  
Milan Krojidlo ◽  
Tomislav Barth ◽  
Karel Jošt

Preparation of oxytocin, arginine-vasopressin and its deamino-analogue serves as an example of use of 2,4,6-trimethylbenzyl group for protection of the cysteine sulfur atom in the peptide synthesis. This modified benzyl group is sufficiently stable under conditions of solvolytic removal of common amino-protecting groups and it can be cleaved off under mild conditions with liquid hydrogen fluoride or trifluoromethanesulfonic acid.


2009 ◽  
Vol 42 (1) ◽  
pp. 10-13 ◽  
Author(s):  
MARIA A. BEDNAREK ◽  
JAMES P. SPRINGER ◽  
BARRY R. CUNNINGHAM ◽  
AMY M. BERNICK ◽  
MIKLOS BODANSZKY

1979 ◽  
Vol 10 (7) ◽  
Author(s):  
L. S. BOGUSLAVSKAYA ◽  
N. B. MELNIKOVA ◽  
A. P. VORONIN ◽  
V. R. KARTASHOV

1999 ◽  
Vol 111 (10) ◽  
pp. 4663-4671 ◽  
Author(s):  
U. Balucani ◽  
D. Bertolini ◽  
G. Sutmann ◽  
A. Tani ◽  
R. Vallauri

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