One-pot synthesis of heterocycle-fused 1,3-diselenole-2-selones as the key precursors of tetraselenafulvalene-type electron donors

Atsushi Morikami, Kazuo Takimiya, Yoshio Aso, Tetsuo Otsubo

Research output: Contribution to journalArticlepeer-review

15 Citations (Scopus)

Abstract

(equation presented) X = S, Se; n = 1-3 A simple one-pot synthetic method of a series of 4,5-alkylenedichalcogeno-substituted 1,3-diselenole-2-selones by successive treatments of trimethylsilylacetylene with butyllithium, selenium, carbon diselenide, and finally α,ω-bis(chalcogenocyanato)alkanes is described.

Original languageEnglish
Pages (from-to)23-25
Number of pages3
JournalOrganic letters
Volume1
Issue number1
DOIs
Publication statusPublished - 1999 Jul 15
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

Fingerprint Dive into the research topics of 'One-pot synthesis of heterocycle-fused 1,3-diselenole-2-selones as the key precursors of tetraselenafulvalene-type electron donors'. Together they form a unique fingerprint.

Cite this