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Synthesis of diaste...
Synthesis of diastereo- and enantiomerically pure anti-3-methyl-1,4-pentanediol via lipase catalysed acylation : Tetrahedron: Asymmetry
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Lindström, Mona (author)
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- Hedenström, Erik (author)
- Mittuniversitetet,Institutionen för naturvetenskap (-2008)
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Bouilly, S (author)
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Velonia, K (author)
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Smonou, I (author)
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(creator_code:org_t)
- Elsevier BV, 2005
- 2005
- English.
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In: Tetrahedron: Asymmetry. - : Elsevier BV. - 0957-4166. ; 16:7, s. 1355-1360
- 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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- Racemic trans-4,5-dimethylhydrofuran-2(3H)-one was synthesised from 5-methyl-furan-2(3H)-one, (alpha-angelica lactone). The key reaction in the synthesis was the 1,4-conjugate addition of an organocuprate to 5-methylfuran-2(5H)-one (beta-angelica lactone). Different types of organocuprates were tested with the highest anti:syn ratio of 99.4:0.6 being obtained by the use of a Gilman organocuprate reagent. The enantioselective acylation of racemic 3-methyl-pentan-1,4-diol, catalysed by a variety of lipases in organic media, was investigated. The highest enantioselectivity (E > 400) was obtained when Novozyme 435 was used as the catalyst at a water activity of a(w) similar to 0. Thus, both enantiomers, (3S,4R)- and (3R,4S)-3-methyl-pentan-1,4-diol, were obtained in very high diastereomeric (> 99% de) and enantiomeric purities (> 99.8% and > 97.4% ee, respectively).
Subject headings
- NATURVETENSKAP -- Kemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences (hsv//eng)
Keyword
- Lipase
- stereoselective
- synthesis
- Chemistry
- Kemi
Publication and Content Type
- ref (subject category)
- art (subject category)
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