Furannulation strategy. An efficient synthesis of fused 3-methylfurans

Mariko Aso, Mizue Sakamoto, Narumi Urakawa, Ken Kanematsu

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

A two-step synthesis of fused 3-methylfurans (furannulation) by the addition of enolate anion of cyclic 1,3-dicarbonyl compounds to allenic sulfonium salt is described.

Original languageEnglish
Pages (from-to)1003-1006
Number of pages4
JournalHeterocycles
Volume31
Issue number6
Publication statusPublished - Jun 1 1990

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Anions
Salts
3-methylfuran

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Cite this

Aso, M., Sakamoto, M., Urakawa, N., & Kanematsu, K. (1990). Furannulation strategy. An efficient synthesis of fused 3-methylfurans. Heterocycles, 31(6), 1003-1006.

Furannulation strategy. An efficient synthesis of fused 3-methylfurans. / Aso, Mariko; Sakamoto, Mizue; Urakawa, Narumi; Kanematsu, Ken.

In: Heterocycles, Vol. 31, No. 6, 01.06.1990, p. 1003-1006.

Research output: Contribution to journalArticle

Aso, M, Sakamoto, M, Urakawa, N & Kanematsu, K 1990, 'Furannulation strategy. An efficient synthesis of fused 3-methylfurans' Heterocycles, vol. 31, no. 6, pp. 1003-1006.
Aso M, Sakamoto M, Urakawa N, Kanematsu K. Furannulation strategy. An efficient synthesis of fused 3-methylfurans. Heterocycles. 1990 Jun 1;31(6):1003-1006.
Aso, Mariko ; Sakamoto, Mizue ; Urakawa, Narumi ; Kanematsu, Ken. / Furannulation strategy. An efficient synthesis of fused 3-methylfurans. In: Heterocycles. 1990 ; Vol. 31, No. 6. pp. 1003-1006.
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