Towards the biotechnological isomerization of branched sugars: D-tagatose-3-epimerase equilibrates both enantiomers of 4-C-methyl-ribulose with both enantiomers of 4-C-methyl-xylulose

Ижил төстэй зүйлс

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  -н: Jones, N, зэрэг
  Хэвлэсэн: (2008)
• A concise approach to the synthesis of all twelve 5-deoxyhexoses: D-tagatose-3-epimerase-a reagent that is both specific and general
  -н: Rao, D, зэрэг
  Хэвлэсэн: (2009)
• Carbon-branched carbohydrate chirons: practical access to both enantiomers of 2-C-methyl-ribono-1,4-lactone and 2-C-methyl-arabinonolactone
  -н: Booth, K, зэрэг
  Хэвлэсэн: (2008)
• Conversion of L-rhamnose into ten of the sixteen 1-and 6-deoxyketohexoses in water with three reagents: D-tagatose-3-epimerase equilibrates C3 epimers of deoxyketoses
  -н: Gullapalli, P, зэрэг
  Хэвлэсэн: (2010)
• Doubly carbon-branched pentoses: synthesis of both enantiomers of 2.4-di-C-methyl arabinose and 2-deoxy-2,4-di-C-methyl arabinose using only acetonide protection
  -н: Booth, K, зэрэг
  Хэвлэсэн: (2009)