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Volumn 132, Issue 23, 2010, Pages 7998-8009

In situ generated bulky palladium hydride complexes as catalysts for the efficient isomerization of olefins. Selective transformation of terminal alkenes to 2-alkenes

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVE CATALYST; ACYL COMPLEXES; ALLYL ETHERS; ALLYLATIONS; ALTERNATIVE CATALYSTS; CARBON MIGRATION; CATALYST LOADINGS; CATALYTIC SYSTEM; CHLORIDE LIGANDS; EPIMERIZATION; HOMOALLYLIC ALCOHOL; IN-SITU; PALLADIUM HYDRIDE; QUANTITATIVE YIELDS; SELECTIVE TRANSFORMATION; SINGLE CRYSTAL X-RAY STRUCTURES; STEREOGENIC CARBONS; TERMINAL ALKENES; TERMINAL OLEFINS;

EID: 77953313694     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja9108424     Document Type: Article
Times cited : (188)

References (141)
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    • Compound 43 could not be separated from the starting material 35 by column chromatography. See the Supporting Information.
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    • Work regarding the optimization of the one-carbon migration using cataCXium PinCy as ligand is currently ongoing in our laboratories and will be reported in due time
    • Work regarding the optimization of the one-carbon migration using cataCXium PinCy as ligand is currently ongoing in our laboratories and will be reported in due time.
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    • Personal correspondence with Anny Jutand (Ecole Normale Supérieure, Département de Chimie, URA CNRS 1679, 24 rue Lhomond, 75231 Paris, Cedex 05, France)
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    • 4 also provided an active catalyst (Table 4, entry 2)
    • 4 also provided an active catalyst (Table 4, entry 2).
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    • 2 and isobutyryl chloride does not provide an active catalyst in control experiments, suggesting that the catalytically active species carries at least one phosphine ligand.


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