124394-58-7Relevant academic research and scientific papers
Helical pores self-assembled from homochiral dendritic dipeptides based on L-Tyr and nonpolar α-amino acids
Percec, Virgil,Dulcey, Andres E.,Peterca, Mihai,Adelman, Peter,Samant, Ritika,Balagurusamy, Venkatachalapathy S. K.,Heiney, Paul A.
, p. 5992 - 6002 (2007)
The synthesis of dendritic dipeptides (4-3,4-3,5)12G2-CH 2-Boc-L-Tyr-X-OMe where X = Gly, L-Val, L-Leu, L-lle, L-Phe, and L-Pro is reported. Their self-assembly in bulk and in solution and the structural and retrostructural analysis of their pe
Marine natural occurring 2,5-diketopiperazines: Isolation, synthesis and optical properties
Laville, Rmi,Nguyen, Thanh Binh,Moriou, Cline,Petek, Sylvain,Debitus, Ccile,Al-Mourabit, Ali
, p. 1351 - 1366 (2015/03/04)
Seven 2,5-diketopiperazines (DKPs) were isolated from the Fijian marine sponge Acanthella cavernosa. NMR and circular dichroism (CD) comparison with synthetic L-L DKPs allowed us to determine unambiguously the L-L absolute configuration of the natural DKPs. This work initiated the setting up of an optical properties database of natural DKPs, including specific rotation and CD.
SYNTHESIS OF THE N-TERMINAL TRIPEPTIDE OF THE OXYTOCIN SEQUENCE
Ivanov, A. K.,Karel'skii, V. N.,Krysin, E. P.,Lavut, E. E.,Zel'tser, I. E.,Antonov, A. A.
, p. 103 - 108 (2007/10/02)
Two schemes for the synthesis of the hydrazide of the N-terminal tripeptide of the oxytocin sequence are considered.It is shown that the most rational is a 1 + 2 scheme.
