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1 s, and show that the complex undergoes Berry pseudorotation.
2 he guanidinium promoted activation energy of pseudorotation.
3 cdG deoxyribose exhibited the O4'-exo (west) pseudorotation.
4 further evidence suggests a role for ribosyl pseudorotation.
5 through a low-lying TBP transition state for pseudorotation.
6                                  Comparative pseudorotation analyses of the J-coupling data for this
7 er VSC, which showed two competing channels: pseudorotation and intramolecular vibrational-energy red
8  analytically described using the concept of pseudorotation, and for RNA and DNA they are dominated b
9          The two populations differed in the pseudorotation angle of the sugar ring for the 5'-neighb
10 kbone conformational variables such as sugar pseudorotation angles and BI/BII state equilibria and th
11                            The altered sugar pseudorotation at A6 appears to be common to both bay re
12 hanisms involving two, four, and three Berry pseudorotations at phosphorus, respectively.
13  the south (B form) sugar pucker to the east pseudorotation barrier are lower in pyrimidines as compa
14 ll accelerated, with IVR becoming faster and pseudorotation being slowed down.
15 ded RNAs to sample a wider spectrum of their pseudorotation conformations.
16 only the relative stability of the different pseudorotation conformers, but also the main transition
17 graphy, and their structures (which span the pseudorotation coordinate between trigonal bipyramidal a
18  onto the productive [2 + 2] cycloreversion; pseudorotation corrects this handicap and makes catalyti
19 nts, a free energy landscape of the complete pseudorotation cycle of nucleic acids in solution has re
20 pared with those outside of the cavity, with pseudorotation dominating.
21                   Results show that the east pseudorotation energy barrier involves a decrease in the
22 calculated the free energy surface of ribose pseudorotation in guanosine and 2'-deoxyguanosine.
23                                              Pseudorotation in the all-cis boat isomer (3) proceeds w
24 cal mol(-1), ruling out a mechansm via Berry pseudorotation involving equatorial halides.
25 entified a cis-trans isomerization via Berry-pseudorotation involving one of the pendant ether groups
26                         However, the O4'-exo pseudorotation of the S-cdG deoxyribose perturbed the he
27 ular dynamics (MD) simulations using the two pseudorotation parameters directly as the collective var
28 ne following the 5'-5' linkage, the C3'- exo pseudorotation phase angle of the alpha-nucleotide, and
29  through the selenium center and for various pseudorotation processes.
30 amer was used to re-evaluate the deoxyribose pseudorotation profile and the Lennard-Jones nonbonded e
31 steep distance-dependent form, a deoxyribose pseudorotation profile with reduced energy barriers betw
32 f the atoms in the furanose ring in terms of pseudorotation puckering amplitude (q) and the pseudorot
33 ters, including the diffusion coefficient D, pseudorotation puckering amplitude q, and the form of th
34 eudorotation puckering amplitude (q) and the pseudorotation puckering phase phi.
35 ffect on the dynamics of the Fe(CO)(5) Berry pseudorotation reaction for comparison to recent two-dim
36 he north and south ranges of the deoxyribose pseudorotation surfaces have been located, allowing char
37      The underlying mechanism is a molecular pseudorotation that can be triggered by infrared pulses
38 est energy structure, which can rearrange by pseudorotation through the T geometry.