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Catalytic activation of hydrogen, silicon, and fluorine by transition-metal complexes

Abstract:
The remarkable versatility of palladium catalysis is exemplified by recent work in two distinct areas. Firstly, coupling chemistry is discussed, in which the reactive entity is generated by cleavage of a C-H or C-Si bond. The second part concerns the activation of allylic C-F bonds, where divergence from the normal stereochemical pattern of the reaction was observed. © 2010 IUPAC.
Publication status:
Published

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Publisher copy:
10.1351/PAC-CON-09-10-37

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Institution:
University of Oxford
Department:
Oxford, MPLS, Chemistry, Organic Chemistry
Volume:
82
Issue:
7
Pages:
1415-1428
Publication date:
2010-07-05
DOI:
EISSN:
1365-3075
ISSN:
0033-4545
URN:
uuid:44b24446-db16-4457-b634-3c0be000af0e
Source identifiers:
65953
Local pid:
pubs:65953

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