Tert-Butyl N-(4-Aminopyridin-2

Synthesis of Peptides Using Tert-Butyloxycarbonyl (Boc) as the -Amino Protection Group

The use of the tert -butyloxycarbonyl (Boc) as the N α-amino protecting group in peptide synthesis can be advantageous in several cases, such as synthesis of hydrophobic peptides and peptides containing ester and thioester moieties

Two‐Step, One‐Pot Synthesis of Inosine, Guanosine, and 2′‐Deoxyguanosine O6‐Ethers via Intermediate O6‐(Benzotriazol‐1‐yl) Derivatives

N‐/purin‐6‐yl/pyridinium salts. Nucleic Acids Res. 13:2989‐3003.    Allerson, C.R., Chen, S.L., and Verdine, G.L. 1997. A chemical method for site‐specific modification

Determination of Sulfur Amino Acids, Glutathione, and Related Aminothiols in Biological Samples by Gas Chromatography with Flame Photometric Detection

and lack sensitivity. GC methods based on the conversion into trimethylsilyl (4 ,5 ), neopentylidine (6 ), and N-trifluoroacetyl n -butyl ester (7 ) derivatives lack sensitivity, gives a tailing peak and requires anhydrous derivatization conditions