Asymmetric synthesis of bis-tetrahydrofuran cores in annonaceous acetogenins

Chia Hsiu Chen; Ting Chun Kuan; Ke Jhen Lu; Duen Ren Hou

doi:10.1039/c004672h

Asymmetric synthesis of bis-tetrahydrofuran cores in annonaceous acetogenins

Chia Hsiu Chen, Ting Chun Kuan, Ke Jhen Lu, Duen Ren Hou

化學學系

研究成果: 雜誌貢獻 › 期刊論文 › 同行評審

4 引文斯高帕斯（Scopus）

摘要

The bis-THF cores of annonaceous acetogenins were synthesized using (3R,4R)-1,5-hexadiene-3,4-diol (1) as the sole source of carbon atoms. The methylene acetal function was applied as a new linker/tether to facilitate the ring-closing metathesis.

原文	???core.languages.en_GB???
頁（從 - 到）	3624-3626
頁數	3
期刊	Organic and Biomolecular Chemistry
卷	8
發行號	16
DOIs	https://doi.org/10.1039/c004672h
出版狀態	已出版 - 21 8月 2010

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10.1039/c004672h

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AU - Chen, Chia Hsiu

AU - Kuan, Ting Chun

AU - Lu, Ke Jhen

AU - Hou, Duen Ren

PY - 2010/8/21

Y1 - 2010/8/21

N2 - The bis-THF cores of annonaceous acetogenins were synthesized using (3R,4R)-1,5-hexadiene-3,4-diol (1) as the sole source of carbon atoms. The methylene acetal function was applied as a new linker/tether to facilitate the ring-closing metathesis.

AB - The bis-THF cores of annonaceous acetogenins were synthesized using (3R,4R)-1,5-hexadiene-3,4-diol (1) as the sole source of carbon atoms. The methylene acetal function was applied as a new linker/tether to facilitate the ring-closing metathesis.

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U2 - 10.1039/c004672h

DO - 10.1039/c004672h

M3 - 期刊論文

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JO - Organic and Biomolecular Chemistry

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Asymmetric synthesis of bis-tetrahydrofuran cores in annonaceous acetogenins

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