Regioselective acylation of 1,6-anhydro-β-D-manno and galactopyranose catalysed by lipases

Tetrahedron: Asymmetry

Volumn 6, Issue 6, 1995, Pages 1387-1392

  Junot, N ^a   Meslin, J C ^a   Rabiller, C ^a  

^a Centre National de la Recherche Scientifique   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CARBOHYDRATE DERIVATIVE; TRIACYLGLYCEROL LIPASE;

ACYLATION; ARTICLE; ENANTIOMER; ENZYME ACTIVITY; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; PSEUDOMONAS;

EID: 0029017814     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/0957-4166(95)00171-K     Document Type: Article

References (23)

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5. Enzyme-catalysed partial deacylation of 1,6-anhydro-2,3,4-tri-O-butyryl-β-D-glucopyranose in the presence of methanol
6. Enzyme-catalyzed partial deacetylation of 1,6-anhydro-2,3,4-tri-O-acetyl-β-D-glucopyranose
7. Two Syntheses of 3-Azido-3-deoxy-D-mannose
8. A practical, efficient large-scale synthesis of 1,6-anhydrohexopyranoses
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10. The allyl ether as a protecting group in carbohydrate chemistry. Part IX. Synthesis of derivatives of 1,6-anhydro-?-D-galactopyranose
11. NMR-Spektren von 1.6-Anhydro-β-D-hexopyranosen
12. Configurational effects on13C chemical shifts of 1,6-anhydro-hexopyranoses and related compounds. Utility of13C–1H coupling patterns for signal assignments