On the Structure of Liquid Hydrogen Fluoride.

ChemInform ◽  
2004 ◽  
Vol 35 (24) ◽  
Author(s):  
Sylvia E. McLain ◽  
Chris J. Benmore ◽  
Joan E. Siewenie ◽  
Jacob Urquidi ◽  
John F. C. Turner
2004 ◽  
Vol 43 (15) ◽  
pp. 1952-1955 ◽  
Author(s):  
Sylvia E. McLain ◽  
Chris J. Benmore ◽  
Joan E. Siewenie ◽  
Jacob Urquidi ◽  
John F. C. Turner

2004 ◽  
Vol 116 (15) ◽  
pp. 1986-1989 ◽  
Author(s):  
Sylvia E. McLain ◽  
Chris J. Benmore ◽  
Joan E. Siewenie ◽  
Jacob Urquidi ◽  
John F. C. Turner

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

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