79083-38-8Relevant articles and documents
Synthesis, conformational analysis and biological studies of cyclic cationic antimicrobial peptides containing sugar amino acids
Chakraborty, Tushar Kanti,Koley, Dipankar,Ravi, Rapolu,Krishnakumari, Viswanatha,Nagaraj, Ramakrishnan,Kunwar, Ajit Chand
experimental part, p. 8731 - 8744 (2009/04/11)
(Chemical Equation Presented) Sugar amino acid based 24-membered macrocyclic C2-symmetric cationic peptides were designed and synthesized. The cationic group was introduced in the sugar amino acids. The conformation of these cyclic compounds was ascertain
Alkylalanes and methyl furanosides: regioselective O-debenzylation or acetal cleavage
Jia, Cai,Zhang, Yongmin,Zhang, Li-He,Sinay, Pierre,Sollogoub, Matthieu
, p. 2135 - 2144 (2007/10/03)
Perbenzylated methyl pentofuranosides were submitted to the action of three alkylalanes and regioselective debenzylation at O-2 of the four pentoses was observed when choosing the right match between anomeric configuration and aluminium reagent. Diisobuty
An epoxide derived from D-glucose as the key intermediate for penaresidine and sphingolipids synthesis
Beauhaire, Josiane,Ducrot, Paul-Henri
, p. 2443 - 2456 (2007/10/03)
A multigram-scale synthesis of 3R,4R,5R 3,5-dibenzyloxy-4-p- methoxybenzyl-1,2-epoxypentane and its use as intermediate for sphingolipids, penazeridine and penazetidine synthesis are described.