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Biaryl phosphite-ox...
Biaryl phosphite-oxazolines from hydroxyl aminoacid derivatives: highly efficient modular ligands for Ir-catalyzed hydrogenation of alkenes
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Diéguez, Montserrat (author)
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Mazuela, Javier (author)
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Pàmies, Oscar (author)
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- Verendel, Johan (author)
- Uppsala universitet,Organisk kemi I
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- Andersson, Pher (author)
- Uppsala universitet,Organisk kemi I
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(creator_code:org_t)
- Royal Society of Chemistry (RSC), 2008
- 2008
- English.
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In: Chemical Communications. - : Royal Society of Chemistry (RSC). - 1359-7345 .- 1364-548X. ; :33, s. 3888-3890
- Related links:
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https://urn.kb.se/re...
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https://doi.org/10.1...
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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
Publication and Content Type
- ref (subject category)
- art (subject category)
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