Im-trityl protection of histidine.
S J Harding, J H Jones, A N Sabirov, V V Samukov
Index: J. Pept. Sci. 5(8) , 368-73, (1999)
Full Text: HTML
Abstract
A rational attempt to prepare FmocHis(piTrt)OH regiospecifically gave in fact the well-known tau-trityl isomer, and experiments with model systems indicate that the prospects for access to pi-trityl histidine derivatives, which would be of great value for the racemization-free synthesis of histidine-containing peptides, are poor.
Related Compounds
Related Articles:
2008-03-13
[J. Med. Chem. 51 , 1115-25, (2008)]
2014-01-01
[Nat. Commun. 5 , 5131, (2014)]
Comparative susceptibility of newborn and young rats to six industrial chemicals.
2005-12-01
[Congenit. Anom. (Kyoto.) 45(4) , 137-45, (2005)]
2006-04-01
[Biochim. Biophys. Acta 847(1) , 1-7, (1985)]
Method for activation and recycling of trityl resins.
2012-08-17
[J. Org. Chem. 77(16) , 7071-5, (2012)]