Justicia lignans

Part 10-Synthesis of tiruneesiin, the first neolignan from Justicia species

Gottumukkala V. Subbaraju, Jakka Kavitha, Dodda Rajasekhar, Feng L. Hsu, Kur T. Cheng

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

(±)-Tiruneesiin, 3-[2-(4-hydroxy-3-methoxyphenyl)-3-acetoxymethyl-7- methoxy-2, 3-dihydro-1-benzofuran-5-yl]propan-1-yl acetate 1, is synthesized starting from methyl ferulate 2 with an overall yield of 12.6%. Ag2O induced dimerization of 2 is used as a key step in the synthesis.

Original languageEnglish
Pages (from-to)357-359
Number of pages3
JournalIndian Journal of Chemistry - Section B Organic and Medicinal Chemistry
Volume46
Issue number2
Publication statusPublished - Feb 2007

Fingerprint

Justicia
Lignans
Dimerization
Acetates
methyl ferulate
1-benzofuran

Keywords

  • Justicia neesii
  • Neolignan
  • Oxidative dimerization
  • Synthesis
  • Tiruneesiin

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Justicia lignans : Part 10-Synthesis of tiruneesiin, the first neolignan from Justicia species. / Subbaraju, Gottumukkala V.; Kavitha, Jakka; Rajasekhar, Dodda; Hsu, Feng L.; Cheng, Kur T.

In: Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, Vol. 46, No. 2, 02.2007, p. 357-359.

Research output: Contribution to journalArticle

Subbaraju, Gottumukkala V. ; Kavitha, Jakka ; Rajasekhar, Dodda ; Hsu, Feng L. ; Cheng, Kur T. / Justicia lignans : Part 10-Synthesis of tiruneesiin, the first neolignan from Justicia species. In: Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry. 2007 ; Vol. 46, No. 2. pp. 357-359.
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AU - Hsu, Feng L.

AU - Cheng, Kur T.

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