Synthesis of the liposidomycin diazepanone nucleoside

Spencer Knapp, Gregori J. Morriello, George A. Doss

Research output: Contribution to journalArticlepeer-review

39 Scopus citations

Abstract

(formula presented) The synthesis of the liposidomycin degradation product 4 from D-glucose establishes its stereochemistry as 5′S,6′S and, by incorporation of the earlier diazepanone relative stereochemical assignment, establishes the absolute stereochemistry of the liposidomycins 1 and 2 as 5′S,6′S,2‴S,3‴S.

Original languageEnglish (US)
Pages (from-to)603-606
Number of pages4
JournalOrganic letters
Volume4
Issue number4
DOIs
StatePublished - Feb 21 2002

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

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