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Reductive Ring Open...
Reductive Ring Openings of Carbohydrate Benzylidene Acetals Using Borane-Trimethylamine and Aluminium Chloride. Regioselectivity and Solvent Dependance
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- Monica, Ek (author)
- KTH,Träkemi och massateknologi
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Garegg, Per J (author)
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Hultberg, Hans (author)
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Oscarson, Stefan (author)
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(creator_code:org_t)
- 1983
- 1983
- English.
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In: Journal of carbohydrate chemistry. - 0732-8303 .- 1532-2327. ; 2:3, s. 305-311
- Related links:
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https://urn.kb.se/re...
Abstract
Subject headings
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- Regioselective reductive ring openings of 4, 6-O-benzylidene acetals of hexopyranosides are described using borane trimethylamine-aluminium chloride. Using toluene as solvent, 4-O-benzyl ethers with the 6-OH free are obtained. Using tetrahydrofuran as solvent. 6-O-benzyl ethers with the 4-OH free are obtained.
Subject headings
- TEKNIK OCH TEKNOLOGIER -- Kemiteknik -- Polymerteknologi (hsv//swe)
- ENGINEERING AND TECHNOLOGY -- Chemical Engineering -- Polymer Technologies (hsv//eng)
- NATURVETENSKAP -- Kemi -- Polymerkemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences -- Polymer Chemistry (hsv//eng)
Publication and Content Type
- ref (subject category)
- art (subject category)
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