6-Deoxyhexoses from l-Rhamnose in the Search for Inducers of the Rhamnose Operon: Synergy of Chemistry and Biotechnology.

نویسندگان

  • Zilei Liu
  • Akihide Yoshihara
  • Ciarán Kelly
  • John T Heap
  • Mikkel H S Marqvorsen
  • Sarah F Jenkinson
  • Mark R Wormald
  • José M Otero
  • Amalia Estévez
  • Atsushi Kato
  • George W J Fleet
  • Ramón J Estévez
  • Ken Izumori
چکیده

In the search for alternative non-metabolizable inducers in the l-rhamnose promoter system, the synthesis of fifteen 6-deoxyhexoses from l-rhamnose demonstrates the value of synergy between biotechnology and chemistry. The readily available 2,3-acetonide of rhamnonolactone allows inversion of configuration at C4 and/or C5 of rhamnose to give 6-deoxy-d-allose, 6-deoxy-d-gulose and 6-deoxy-l-talose. Highly crystalline 3,5-benzylidene rhamnonolactone gives easy access to l-quinovose (6-deoxy-l-glucose), l-olivose and rhamnose analogue with C2 azido, amino and acetamido substituents. Electrophilic fluorination of rhamnal gives a mixture of 2-deoxy-2-fluoro-l-rhamnose and 2-deoxy-2-fluoro-l-quinovose. Biotechnology provides access to 6-deoxy-l-altrose and 1-deoxy-l-fructose.

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عنوان ژورنال:
  • Chemistry

دوره 22 35  شماره 

صفحات  -

تاریخ انتشار 2016