Skeletal Reorganization: Synthesis of Diptoindonesin G from Pauciflorol F

Dileep Kumar Singh, Ikyon Kim

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Described herein is a novel synthetic approach to diptoindonesin G, a highly potent anticancer oligostilbenoid natural product, from pauciflorol F pentamethyl ether through a skeletal reorganization strategy where oxidative cleavage of the indanone ring system of pauciflorol F and sequential cyclization of the key intermediate allowed direct access to the target skeleton.

Original languageEnglish
Pages (from-to)1667-1672
Number of pages6
JournalJournal of Organic Chemistry
Volume83
Issue number3
DOIs
Publication statusPublished - 2018 Feb 2

Fingerprint

Cyclization
Biological Products
Ether
pauciflorol F
diptoindonesin G
indacrinone

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Cite this

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abstract = "Described herein is a novel synthetic approach to diptoindonesin G, a highly potent anticancer oligostilbenoid natural product, from pauciflorol F pentamethyl ether through a skeletal reorganization strategy where oxidative cleavage of the indanone ring system of pauciflorol F and sequential cyclization of the key intermediate allowed direct access to the target skeleton.",
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Skeletal Reorganization : Synthesis of Diptoindonesin G from Pauciflorol F. / Singh, Dileep Kumar; Kim, Ikyon.

In: Journal of Organic Chemistry, Vol. 83, No. 3, 02.02.2018, p. 1667-1672.

Research output: Contribution to journalArticle

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