Pentathiomonoorthooxalates

P. Herczegh, Martina Zsély, László Szilágyi

Research output: Contribution to journalArticle

Abstract

Reaction of trialkyl trithioorthoformate anions with carbon disulphide and subsequent methylation of the products gave methyl tris-alkylthio-dithioacetates (pentathiomonoorthooxalates). Attempted Diels-Alder reaction of this new species gave rise to open-chain hexa-1,4Z-dienes 6a-c instead of the expected thiopyran adducts.

Original languageEnglish
Pages (from-to)2063-2066
Number of pages4
JournalTetrahedron
Volume44
Issue number7
DOIs
Publication statusPublished - 1988

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Carbon Disulfide
Methylation
Cycloaddition Reaction
Anions
thiopyran

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Pentathiomonoorthooxalates. / Herczegh, P.; Zsély, Martina; Szilágyi, László.

In: Tetrahedron, Vol. 44, No. 7, 1988, p. 2063-2066.

Research output: Contribution to journalArticle

Herczegh, P, Zsély, M & Szilágyi, L 1988, 'Pentathiomonoorthooxalates', Tetrahedron, vol. 44, no. 7, pp. 2063-2066. https://doi.org/10.1016/S0040-4020(01)90349-7
Herczegh, P. ; Zsély, Martina ; Szilágyi, László. / Pentathiomonoorthooxalates. In: Tetrahedron. 1988 ; Vol. 44, No. 7. pp. 2063-2066.
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