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

5 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

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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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.",

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

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AU - Kim, Ikyon

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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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M3 - Article

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JO - Tetrahedron Letters

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Convergent synthesis of diptoindonesin G

Abstract

Bibliographical note

All Science Journal Classification (ASJC) codes

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