79083-39-9Relevant 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
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.
A facile synthesis of 1,2-anhydroglycofuranose benzyl ethers
Yuguo, Du,Fanzuo, Kong
, p. 427 - 430 (2007/10/02)
The synthesis of 1,2-anhydromanno-, -lyxo-, -gluco-, and -xylofuranose benzyl ethers was successfully achieved via intramolecular S(N)2 reaction of the corresponding C-1 alkoxide with C-2 bearing tosyloxy group. The key intermediates, furanose 2-sulfonate