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Third-Generation Am...
Third-Generation Amino Acid Furanoside-Based Ligands from d-Mannose for the Asymmetric Transfer Hydrogenation of Ketones : Catalysts with an Exceptionally Wide Substrate Scope
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Margalef, Jessica (author)
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- Slagbrand, Tove (author)
- Stockholms universitet,Institutionen för organisk kemi
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- Tinnis, Fredrik (author)
- Stockholms universitet,Institutionen för organisk kemi
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- Adolfsson, Hans (author)
- Stockholms universitet,Umeå universitet,Kemiska institutionen,Stockholm University,Department of Organic Chemistry,Arrheniuslaboratoriet SE-106 91 Stockholm,Sweden,Institutionen för organisk kemi,Umeå University, Sweden
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Dieguez, Montserrat (author)
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Pamies, Oscar (author)
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(creator_code:org_t)
- 2016-12-07
- 2016
- English.
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In: Advanced Synthesis and Catalysis. - : Wiley. - 1615-4150 .- 1615-4169. ; 358:24, s. 4006-4018
- Related links:
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https://urn.kb.se/re...
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https://doi.org/10.1...
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https://urn.kb.se/re...
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Abstract
Subject headings
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- A modular ligand library of -amino acid hydroxyamides and thioamides was prepared from 10 different N-tert-butyloxycarbonyl-protected -amino acids and three different amino alcohols derived from 2,3-O-isopropylidene--d-mannofuranoside. The ligand library was evaluated in the half-sandwich ruthenium- and rhodium-catalyzed asymmetric transfer hydrogenation of a wide array of ketone substrates, including simple as well as sterically demanding aryl alkyl ketones, aryl fluoroalkyl ketones, heteroaromatic alkyl ketones, aliphatic, conjugated and propargylic ketones. Under the optimized reaction conditions, secondary alcohols were obtained in high yields and in enantioselectivities up to >99%. The choice of ligand/catalyst allowed for the generation of both enantiomers of the secondary alcohols, where the ruthenium-hydroxyamide and the rhodium-thioamide catalysts act complementarily towards each other. The catalytic systems were also evaluated in the tandem isomerization/asymmetric transfer hydrogenation of racemic allylic alcohols to yield enantiomerically enriched saturated secondary alcohols in up to 98% ee. Furthermore, the catalytic tandem -alkylation/asymmetric transfer hydrogenation of acetophenones and 3-acetylpyridine with primary alcohols as alkylating and reducing agents was studied. Secondary alcohols containing an elongated alkyl chain were obtained in up to 92% ee.
Subject headings
- NATURVETENSKAP -- Kemi -- Organisk kemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences -- Organic Chemistry (hsv//eng)
- NATURVETENSKAP -- Kemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences (hsv//eng)
Keyword
- asymmetric transfer hydrogenation
- hydroxyamide ligands
- rhodium
- ruthenium
- sugar-based ligands
- ndem reactions
- thioamide ligands
Publication and Content Type
- ref (subject category)
- art (subject category)
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