Syntheses of heliannuols G and H; structure revision of the natural products

Sachie Morimoto; Mitsuru Shindo; Masahiro Yoshida; Kozo Shishido

doi:10.1016/j.tetlet.2006.08.014

Syntheses of heliannuols G and H; structure revision of the natural products

Sachie Morimoto, Mitsuru Shindo, Masahiro Yoshida, Kozo Shishido

Department of Fundamental Organic Chemistry

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

22 Citations (Scopus)

Abstract

The structures of the natural heliannuols G and H were established by the enantiocontrolled syntheses of the dihydrobenzofurans predicted for the natural products employing the palladium-mediated cyclization and cross metathesis as the key steps.

Original language	English
Pages (from-to)	7353-7356
Number of pages	4
Journal	Tetrahedron Letters
Volume	47
Issue number	41
DOIs	https://doi.org/10.1016/j.tetlet.2006.08.014
Publication status	Published - Oct 9 2006

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/j.tetlet.2006.08.014

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title = "Syntheses of heliannuols G and H; structure revision of the natural products",

abstract = "The structures of the natural heliannuols G and H were established by the enantiocontrolled syntheses of the dihydrobenzofurans predicted for the natural products employing the palladium-mediated cyclization and cross metathesis as the key steps.",

author = "Sachie Morimoto and Mitsuru Shindo and Masahiro Yoshida and Kozo Shishido",

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AU - Morimoto, Sachie

AU - Shindo, Mitsuru

AU - Yoshida, Masahiro

AU - Shishido, Kozo

PY - 2006/10/9

Y1 - 2006/10/9

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AB - The structures of the natural heliannuols G and H were established by the enantiocontrolled syntheses of the dihydrobenzofurans predicted for the natural products employing the palladium-mediated cyclization and cross metathesis as the key steps.

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M3 - Article

AN - SCOPUS:33748322027

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SP - 7353

EP - 7356

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 41

ER -

Syntheses of heliannuols G and H; structure revision of the natural products

Abstract

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