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Memory and dynamics in Pd-catalyzed allylic alkylation with P,N-ligands
被引:23
|作者:
Johansson, Charlotte
[1
]
Lloyd-Jones, Guy C.
[2
]
Norrby, Per-Ola
[1
]
机构:
[1] Univ Gothenburg, Dept Chem, SE-41296 Gothenburg, Sweden
[2] Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
基金:
瑞典研究理事会;
关键词:
CONTINUUM DIELECTRIC THEORY;
ASYMMETRIC CATALYSIS;
PALLADIUM(0) COMPLEXES;
(ETA-3-ALLYL)PALLADIUM COMPLEXES;
(PI-ALLYL)PALLADIUM COMPLEXES;
SELECTIVE STABILIZATION;
OXIDATIVE ADDITION;
CHLORIDE-IONS;
SUBSTITUTION;
LIGANDS;
D O I:
10.1016/j.tetasy.2010.03.031
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
The memory effect, known to exert a strong influence on selectivity in some applications of the Pd-catalyzed allylic alkylation, has been investigated for a catalytic system based on a bidentate P,N-ligand. Although this system might be expected to show strong memory effects due to the difference in the trans influence of the two donor atoms (P > N), isotopic labeling revealed an almost complete absence of regio-retention. Modeling of dynamic processes in the intermediate (eta(3)-allyl)Pd complex allowed this observation to be rationalized in terms of anion-assisted apparent rotation. The study has allowed seemingly conflicting reports on the behavior of (eta(3)-allyl)Pd systems to be unified by a computational model. (C) 2010 Elsevier Ltd. All rights reserved.
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页码:1585 / 1592
页数:8
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