79432-14-7Relevant articles and documents
9-BBN as a convenient protecting group in functionalisation of hydroxylysine
Syed, Baquer M.,Gustafsson, Tomas,Kihlberg, Jan
, p. 5571 - 5575 (2007/10/03)
9-BBN was used for regioselective protection of the α-amino and α-carboxyl groups of (5R)-5-hydroxy-L-lysine. The resulting 9-BBN complex was then employed in transformations such as N-Cbz protection, azido transfer, O-glycosylation, and O-silylation. Further manipulations led to improved methods for preparation of hydroxylysine and galactosylated hydroxylysine building blocks, suitable for direct use in peptide synthesis under standard Fmoc conditions.
Bone collagen cross-links: An efficient one-pot synthesis of (+)-pyridinoline and (+)-dexoypyridinoline
Adamczyk, MacIej,Johnson, Donald D.,Reddy, Rajarathnam E.
, p. 2289 - 2298 (2007/10/03)
A one-pot reaction of (2S,5R)-(-)-tert-butyl-[(2-tert-butoxycarbonyl)amino]-5-hydroxy-6-aminohexanoate 2b or (S)-(-)-tert-butyl-[(2-tert-butoxycarbonyl)amino]-6-aminohexanoate 2c with (S)-(-)-tert-butyl-6-bromo-[bis-(2-tert-butoxycarbonyl)amino]-5-oxohexa
Total Synthesis and Absolute Configuration of Bengamide A
Chida, Noritaka,Tobe, Takahiko,Okada, Shinsuke,Ogawa, Seiichiro
, p. 1064 - 1066 (2007/10/02)
The first total synthesis of the novel marine natural product, bengamide A 1 is described, revealing the absolute configuration of this compound.
SYNTHESIS OF O-(2-O-α-D-GLUCOPYRANOSYL)-β-D-GALACTOPYRANOSIDE OF OPTICALLY PURE δ-HYDROXY-L-LYSYLGLYCINE AND δ-HYDROXY-L-LYSYLGLYCYL-L-GLUTAMYL-L-ASPARATYLGLYCINE. COMPONENTS OF THE GLOMERULAR BASEMENT MEMBRANE
Koeners, H. J.,Schattenkerk, Cecile,Verhoeven, J. J.,Boom, J. H. van
, p. 1763 - 1771 (2007/10/02)
The application of the levulinyl group as a temporary blocking group for the 2-OH function of galactose proved to be very efficient not only for the introduction of a β- linkage between galactose and the optically pure δ-hydroxy-L-lysylglycine, but also t