Tartraldehydes, 4. Synthesis of D‐ and L‐rhodinose

P. Herczegh, Imre Kovács, Attila László, Z. Dinya, F. Sztaricskai

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

Starting from tartraldehyde derivatives 1 and 2, we prepared the title compounds 6 and 7 via a Wittig‐type chain elongation, protection of the formyl group, simultaneous reduction of the double bond and reductive desulfurization of the dithioacetal function as well as hydrolytic removal of the acetal‐type protective groups.

Original languageEnglish
Pages (from-to)599-600
Number of pages2
JournalLiebigs Annalen der Chemie
Volume1991
Issue number6
DOIs
Publication statusPublished - 1991

Fingerprint

Desulfurization
Elongation
Derivatives
synthesis
elongation

Keywords

  • Antibiotics
  • D‐Rhodinose
  • L‐Rhodinose
  • Plasma spray method
  • Tartraldehyde mercaptals

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Organic Chemistry

Cite this

Tartraldehydes, 4. Synthesis of D‐ and L‐rhodinose. / Herczegh, P.; Kovács, Imre; László, Attila; Dinya, Z.; Sztaricskai, F.

In: Liebigs Annalen der Chemie, Vol. 1991, No. 6, 1991, p. 599-600.

Research output: Contribution to journalArticle

Herczegh, P. ; Kovács, Imre ; László, Attila ; Dinya, Z. ; Sztaricskai, F. / Tartraldehydes, 4. Synthesis of D‐ and L‐rhodinose. In: Liebigs Annalen der Chemie. 1991 ; Vol. 1991, No. 6. pp. 599-600.
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