One-pot synthesis of trans-β-alkylstyrenes

Ju Tsung Liu, Ching Fa Yao

Research output: Contribution to journalArticle

41 Citations (Scopus)

Abstract

One-pot synthesis of (E)-alkenes 5 from the reactions of aldehyde 1 and nitromethane 2 in the acetic acid solution and then with triethylborane 4 in the biphase of diethyl ether and aqueous solution in the presence of oxygen in air was reported. Various (E)-alkenes 7 could also be prepared when different kinds of secondary or tertiary alkyl iodides 6 were used under similar conditions.

Original languageEnglish
Pages (from-to)6147-6150
Number of pages4
JournalTetrahedron Letters
Volume42
Issue number35
DOIs
Publication statusPublished - 2001 Aug 27

Fingerprint

Alkenes
Iodides
Aldehydes
Acetic Acid
Ether
Air
Oxygen
nitromethane
triethylborane

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Cite this

One-pot synthesis of trans-β-alkylstyrenes. / Liu, Ju Tsung; Yao, Ching Fa.

In: Tetrahedron Letters, Vol. 42, No. 35, 27.08.2001, p. 6147-6150.

Research output: Contribution to journalArticle

Liu, Ju Tsung ; Yao, Ching Fa. / One-pot synthesis of trans-β-alkylstyrenes. In: Tetrahedron Letters. 2001 ; Vol. 42, No. 35. pp. 6147-6150.
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