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1 ride product is observed and complicates the regiochemical analysis.
2 eochemical comparisons demonstrated that the regiochemical and enantiofacial selectivity of P-450 2C2
3 its transformation to the final product, the regiochemical and eventual stereochemical outcome of the
4                                              Regiochemical and olefin geometry was controlled in the
5 more complex structures with a high level of regiochemical and stereochemical control.
6  their branching tendencies as well as their regiochemical and stereochemical diversity.
7             Diene substituent effects on the regiochemical and stereochemical outcomes of uncatalyzed
8 iv of DMPU are required to achieve identical regiochemical and stereochemical results.
9                               Structural and regiochemical aspects of the newly synthesized pyrazoles
10                                          The regiochemical assignment is made on the basis of 13C NMR
11                                              Regiochemical comparisons suggest that the CF(2)H radica
12                    The previously unexplored regiochemical consequences for this catalytic, intermole
13   The methodology developed was based on the regiochemical control of the cyclocondensation reaction
14   The methodology developed was based on the regiochemical control of the reaction of 4-acyl-1H-pyrro
15                                         This regiochemical control problem was solved by extension of
16 ent reaction is subject to a lower degree of regiochemical control than the NADPH-dependent reaction.
17  cation radical rearrangements even when the regiochemical control unit is not directly appended to t
18                                  Significant regiochemical control was observed.
19 gh penta-substituted pyridines with complete regiochemical control.
20 igand is uniquely effective at reverting the regiochemical course of nickel-catalyzed reactions of al
21 ion mechanism is proposed to account for the regiochemical course of this reaction.
22 ldup of charge in oxazoline to reconcile the regiochemical differences between Ghosez and Seebach's o
23 iotics in the genus Streptomyces introducing regiochemical diversity into the macrolide ring system,
24 yer of structural variability by introducing regiochemical diversity into the macrolide ring systems.
25 nkage and encompass the otherwise surprising regiochemical dominance by the remote ester on the olefi
26   They highlight general observations on the regiochemical effects of the beta-oxo-auxochrome.
27 d NEOs, providing insights into the observed regiochemical effects of the substituents.
28                                              Regiochemical effects of uridine thiolation were determi
29                                     Finally, regiochemical effects on mechanochemical coupling are ch
30 h arenes, such as indoles, proceed with high regiochemical fidelity with a range of beta-ketoesters a
31 on the pyridine ring, as well as stereo- and regiochemical influences of the 3,6-diazabicyclo[3.2.0]h
32 ntation energies for different linkers yield regiochemical information essential for identification o
33 w that the bimetallic catalysts suppress the regiochemical insertion selectivity exhibited by the mon
34 or access to allocolchicinoids with reversed regiochemical introduction of ring C substituents.
35        These phenomena are attributed to the regiochemical irregularities in the polymers arising fro
36 ar dynamics (RPMD) to account for an unusual regiochemical isotope effect on the regioselectivity of
37  the boron center in order to understand how regiochemical issues influence photophysical and electro
38                      Both stereochemical and regiochemical issues raised in this study provide furthe
39 Our mechanistic probe reveals an interesting regiochemical kinetic resolution process.
40 hose pair of carbonyl groups are amenable to regiochemical manipulation.
41  that excess dietary salt does not alter the regiochemical or stereochemical selectivity of the kidne
42 ation of this sequence to effect the desired regiochemical outcome and its mechanistic underpinnings
43 fer insights into the origin of the observed regiochemical outcome and the utility of the method is h
44 nfluence of steric and electronic effects on regiochemical outcome and, by linking to current mechani
45 the new ligand class enables a complementary regiochemical outcome compared with previously described
46 uglone dienophiles, and there is an opposite regiochemical outcome for Diels-Alder reactions with bet
47 es, a previously unreported and contrasteric regiochemical outcome for the C-H functionalization of e
48                                          The regiochemical outcome is, thus, the opposite of that nor
49      This strategy is the first where either regiochemical outcome may be selected for a broad range
50 eterocycle correlates qualitatively with the regiochemical outcome of halogenation reactions in >80%
51 correlation (HMBC) was used to determine the regiochemical outcome of palladium-catalyzed carbon-carb
52 ethod was also used to correctly predict the regiochemical outcome of the cycloaddition of BTF with 1
53 redictions of TST for rationalization of the regiochemical outcome of the hydroboration reaction mech
54 ontaining alkyne substrates also affects the regiochemical outcome of the PK reaction.
55                           In some cases, the regiochemical outcome of the reaction can be controlled
56 oup also provides the ability to reverse the regiochemical outcome of the reaction, opening the acces
57 failed to explain the solvent dependence and regiochemical outcome of the reaction.
58 lieved to be responsible for the stereo- and regiochemical outcome of the reaction.
59 iarylacetylenes significantly influenced the regiochemical outcome of the reaction.
60                                 The opposite regiochemical outcome of the two processes allows an eas
61                               To explain the regiochemical outcome of these reactions (C-O arylation
62 ronment around the metal center dictates the regiochemical outcome.
63 zed reaction is consistent with the observed regiochemical outcome.
64 copper salt is responsible for the divergent regiochemical outcomes and that the origin of regiodiver
65            This reagent combination provides regiochemical outcomes that are opposite to, or more sel
66 s found to result in significantly different regiochemical outcomes.
67 eir hydrogen atom abstraction mechanisms and regiochemical plasticity with deuterium-labeled substrat
68                    This lack of C(2) vs C(3) regiochemical predictability led to the development of a
69                                The change in regiochemical preference to the meta borylation (dE(meta
70 her give enhanced regiocontrol or invert the regiochemical preference.
71 results also matched experiments in terms of regiochemical preferences in unsymmetrical rearrangement
72              Insights into the mechanism and regiochemical preferences of this reaction are provided
73 e., "soft-soft", interactions in determining regiochemical preferences.
74                               This disparate regiochemical reactivity underscores the potential of ca
75                                              Regiochemical results that deviate from expectation are
76 ed N-heterocyclic carbene ligands allows the regiochemical reversal with unbiased internal alkynes, a
77 nd impart molecular interactions that define regiochemical ring-opening.
78                       Interestingly, typical regiochemical scrambling associated with the C-H activat
79           Furthermore, it was found that the regiochemical sense of the cycloaddition was apparently
80                  Depending on the particular regiochemical substitution and stereochemical configurat
81           In addition, the importance of the regiochemical substitution on the tetrazole was examined
82                        Finally, a remarkable regiochemical switch upon minor structural modification
83 sor, we developed conditions for stereo- and regiochemical transannular cyclizations to synthesize th
84                                          The regiochemical trends are correlated with B3LYP/6-31G* ca
85 o-meta, were systematically explored through regiochemical variation of the aryl halide and aryl boro