Convergent synthesis of diptoindonesin G

Dileep Kumar Singh; Ikyon Kim

doi:10.1016/j.tetlet.2018.12.036

Convergent synthesis of diptoindonesin G

Dileep Kumar Singh, Ikyon Kim

Department of Pharmacy

Research output: Contribution to journal › Article › peer-review

6 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 language	English
Pages (from-to)	300-301
Number of pages	2
Journal	Tetrahedron Letters
Volume	60
Issue number	3
DOIs	https://doi.org/10.1016/j.tetlet.2018.12.036
Publication status	Published - 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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10.1016/j.tetlet.2018.12.036

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author = "Singh, {Dileep Kumar} and Ikyon Kim",

note = "Funding Information: We thank the National Research Foundation of Korea ( NRF-2017R1A2A2A05069364 and NRF-2018R1A6A1A03023718 ) for generous financial support. Publisher Copyright: {\textcopyright} 2018 Elsevier Ltd",

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AU - Kim, Ikyon

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PY - 2019/1/17

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N2 - 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.

AB - 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.

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ER -

Convergent synthesis of diptoindonesin G

Abstract

Bibliographical note

All Science Journal Classification (ASJC) codes

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