Conformational sampling of bioactive conformers: a low-temperature NMR study of15N-Leu–enkephalin

Author(s):  
Pietro Amodeo ◽  
Fred Naider ◽  
Delia Picone ◽  
Teodorico Tancredi ◽  
Piero A. Temussi
2015 ◽  
Vol 592 ◽  
pp. 012042 ◽  
Author(s):  
Y Kawasaki ◽  
R Morioka ◽  
Y Kishimoto ◽  
K Nakamura ◽  
K Nishiyama ◽  
...  

1989 ◽  
Vol 44 (3) ◽  
pp. 288-292 ◽  
Author(s):  
Bernd Wrackmeyer ◽  
Klaus Horchler ◽  
Hong Zhou ◽  
Michael Veith

1,3-Diisopropyl-2,2-dimethyl-1,3,2,4λ2-diazasilastannetidine (1b) and -plumbetidine (2b) are dimeric [(1b)2, (2b)2] in solution. At room temperature the structure of (1b)2 is fluxional. The dynamic behaviour is interpreted - on the basis of 1H. 13C, 29Si and 119Sn NMR data - as an intramolecular process in which the four-membered rings keep their identity. Such a process involves either concerted opening of the two coordinative Sn - N bonds and mutual slippage of the two rings, or consecutive cleavage of one of the coordinative Sn - N bonds and rotation about the other one. At room temperature the dimer (2b)2 is in equilibrium with its monomer 2b, whereas at low temperature the dynamic process corresponds to that established for (1b)2. In solutions which contain a mixture of the dimers (1b)2 and (2b)2, the presence of the mixed dimer 1b/2b can be proved unambiguously by consistent 29Si, 119Sn and 207Pb NMR data.


1981 ◽  
Vol 59 (2) ◽  
pp. 482-489 ◽  
Author(s):  
André A. Pavia ◽  
Sak N. Ung-Chhun

The acid-catalysed mechanism of the reaction using trifluoromethanesulfonic anhydride to synthesize symmetrical 1,1′-glycosyl-glycosides such as trehalose and galacto, manno, arabino, xylo etc. analogues has been elucidated. The authors were able to prove by 19F nmr study at low temperature that the efficiency of the system is due to the peculiar property of trifluoromethanesulfonic acid generated in situ to form a stable, insoluble hydroxonium trifluoromethanesulfonate CF3SO3− H3O+. The procedure satisfies the two necessary conditions for a glycosylation reaction being workable: (i) the presence in catalytic amounts of free acid which is regenerated during the condensation step; (ii) a very efficient trapping of the water liberated during the protonation step which displaces the equilibrium towards the formation of the glycoside. The α-stereoselectivity of the reaction is discussed in terms of anomerisation of the β-anomers on to the thermodynamically more stable α ones, through a cyclic oxonium intermediate.


1983 ◽  
Vol 42 (3) ◽  
pp. 285-293 ◽  
Author(s):  
L. Trahms ◽  
W.D. Klabe ◽  
E. Boroske

2001 ◽  
Vol 39 (S1) ◽  
pp. S81-S90 ◽  
Author(s):  
Maria Rospenk ◽  
Lucjan Sobczyk ◽  
Parwin Schah-Mohammedi ◽  
Hans-Heinrich Limbach ◽  
Nicolai S. Golubev ◽  
...  

2008 ◽  
Vol 403 (5-9) ◽  
pp. 834-836
Author(s):  
M. Weller ◽  
J.L. Gavilano ◽  
A. Sacchetti ◽  
H.R. Ott

1999 ◽  
Vol 68 (2) ◽  
pp. 346-349 ◽  
Author(s):  
Yuji Furukawa ◽  
Shinji Wada ◽  
Tsuyoshi Kajitani ◽  
Shoichi Hosoya

1977 ◽  
Vol 42 (2) ◽  
pp. 484-491 ◽  
Author(s):  
Hidenori Kubo ◽  
Nobuo Kaneshima ◽  
Yoshiaki Hashimoto ◽  
Kazuo Tsuru ◽  
Kazuyoshi Hirakawa

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