Computational NMR of Carbohydrates: Comparison
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Please note this is a comparison between Version 2 by Conner Chen and Version 1 by Leonid Krivdin.

Nowadays, computational NMR is widely used for structural and stereochemical studies of a wide series of carbohydrates including mono-, di-, and polysaccharides together with their functional derivatives. Stereochemical analysis of carbohydrates could mostly be performed by using computational versus experimental 1H and 13C-NMR chemical shifts and spin-spin coupling constants in view of their marked stereochemical dependences providing a new guide in stereochemical structure of carbohydrates together with fundamental factors controlling molecular recognition and catalysis in biochemical systems.

  • computational NMR
  • chemical shift
  • spin-spin coupling constant
  • carbohydrates
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