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Biaryl phosphite-oxazolines from hydroxyl aminoacid derivatives: highly efficient modular ligands for Ir-catalyzed hydrogenation of alkenes

Diéguez, Montserrat (author)
Mazuela, Javier (author)
Pàmies, Oscar (author)
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Verendel, Johan (author)
Uppsala universitet,Organisk kemi I
Andersson, Pher (author)
Uppsala universitet,Organisk kemi I
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 (creator_code:org_t)
Royal Society of Chemistry (RSC), 2008
2008
English.
In: Chemical Communications. - : Royal Society of Chemistry (RSC). - 1359-7345 .- 1364-548X. ; :33, s. 3888-3890
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • High enantioselectivities and activities are achieved in the Ir-catalyzed hydrogenation of several unfunctionalized olefins using modular biaryl phosphite-oxazoline ligands from hydroxyl aminoacid derivatives, the presence of a biaryl phosphite group is crucial to this success.

Subject headings

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)

Keyword

reduction
hydrogenation
diastereoselective syntheses
enantioselective syntheses (incl. cis/trans-isomerism)
polyphenylalkane derivatives
carboxylic acid esters (benzene compounds)
alcohols (benzene compounds)
Chemistry
Kemi

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ref (subject category)
art (subject category)

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Diéguez, Montser ...
Mazuela, Javier
Pàmies, Oscar
Verendel, Johan
Andersson, Pher
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NATURAL SCIENCES
NATURAL SCIENCES
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Chemical Communi ...
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Uppsala University

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