Convergent synthesis of diptoindonesin G

Dileep Kumar Singh, Ikyon Kim

Research output: Contribution to journalArticle

Abstract

A convergent and scalable synthetic route to a tetracyclic oligostilbenoid natural product, diptoindonesin G, is described where Suzuki-Miyaura cross-coupling and intramolecular Friedel-Crafts acylation were employed to construct the central C ring of diptoindonesin G. Two fragments for cross-coupling reaction were readily synthesized with similar efficiency.

LanguageEnglish
Pages300-301
Number of pages2
JournalTetrahedron Letters
Volume60
Issue number3
DOIs
Publication statusPublished - 2019 Jan 17

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Acylation
Cross Reactions
Biological Products
diptoindonesin G

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Cite this

Singh, Dileep Kumar ; Kim, Ikyon. / Convergent synthesis of diptoindonesin G. In: Tetrahedron Letters. 2019 ; Vol. 60, No. 3. pp. 300-301.
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Convergent synthesis of diptoindonesin G. / Singh, Dileep Kumar; Kim, Ikyon.

In: Tetrahedron Letters, Vol. 60, No. 3, 17.01.2019, p. 300-301.

Research output: Contribution to journalArticle

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