Convergent synthesis of diptoindonesin G

Dileep Kumar Singh, Ikyon Kim

Research output: Contribution to journalArticlepeer-review

4 Citations (Scopus)

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.

Original languageEnglish
Pages (from-to)300-301
Number of pages2
JournalTetrahedron Letters
Volume60
Issue number3
DOIs
Publication statusPublished - 2019 Jan 17

Bibliographical note

Funding Information:
We thank the National Research Foundation of Korea ( NRF-2017R1A2A2A05069364 and NRF-2018R1A6A1A03023718 ) for generous financial support.

Publisher Copyright:
© 2018 Elsevier Ltd

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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