Absolute stereochemistry and preferred conformations of urate degradation intermediates from computed and experimental circular dichroism spectra

2011 ◽  
Vol 9 (14) ◽  
pp. 5149-5155 ◽  
Author(s):  
Silvio Pipolo ◽  
Riccardo Percudani ◽  
Roberto Cammi
2016 ◽  
Vol 14 (14) ◽  
pp. 3654-3654
Author(s):  
Silvio Pipolo ◽  
Riccardo Percudani ◽  
Roberto Cammi

Correction for ‘Absolute stereochemistry and preferred conformations of urate degradation intermediates from computed and experimental circular dichroism spectra’ by Silvio Pipolo et al., Org. Biomol. Chem., 2011, 9, 5149–5155.


1981 ◽  
Vol 59 (15) ◽  
pp. 2303-2305 ◽  
Author(s):  
M. J. Stillman ◽  
J. B. Stothers ◽  
A. Stoess

Application of the exciton chirality method has confirmed that capsidiol, a unique eremophilane, has the absolute stereochemistry depicted in 1. The 1H and 13Cmr, circular dichroism, and magnetic circular dichroism spectra of capsidiol and 1-epicapsidiol dibenzoates are discussed.


1968 ◽  
Vol 65 ◽  
pp. 146-151 ◽  
Author(s):  
G. Scheibe ◽  
O. Wörz ◽  
F. Haimerl ◽  
W. Seiffert ◽  
J. Winkler

RSC Advances ◽  
2021 ◽  
Vol 11 (14) ◽  
pp. 8411-8419
Author(s):  
Jakub Kaminský ◽  
Valery Andrushchenko ◽  
Petr Bouř

Electronic absorption, natural and magnetic circular dichroism spectra of several nucleosides are simulated to understand their dependence on molecular dynamics and environment, their sensitivity to nucleoside pairing and stacking in nucleic acids.


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