One-pot synthesis of trans-β-alkylstyrenes

Ju Tsung Liu; Ching Fa Yao

doi:10.1016/S0040-4039(01)01185-6

One-pot synthesis of trans-β-alkylstyrenes

Ju Tsung Liu, Ching Fa Yao^*

^*此作品的通信作者

化學系

研究成果: 雜誌貢獻 › 期刊論文 › 同行評審

42 引文斯高帕斯（Scopus）

摘要

One-pot synthesis of (E)-alkenes 5 from the reactions of aldehyde 1 and nitromethane 2 in the acetic acid solution and then with triethylborane 4 in the biphase of diethyl ether and aqueous solution in the presence of oxygen in air was reported. Various (E)-alkenes 7 could also be prepared when different kinds of secondary or tertiary alkyl iodides 6 were used under similar conditions.

原文	英語
頁（從 - 到）	6147-6150
頁數	4
期刊	Tetrahedron Letters
卷	42
發行號	35
DOIs	https://doi.org/10.1016/S0040-4039(01)01185-6
出版狀態	已發佈 - 2001 8月 27

ASJC Scopus subject areas

生物化學
藥物發現
有機化學

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10.1016/S0040-4039(01)01185-6

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title = "One-pot synthesis of trans-β-alkylstyrenes",

abstract = "One-pot synthesis of (E)-alkenes 5 from the reactions of aldehyde 1 and nitromethane 2 in the acetic acid solution and then with triethylborane 4 in the biphase of diethyl ether and aqueous solution in the presence of oxygen in air was reported. Various (E)-alkenes 7 could also be prepared when different kinds of secondary or tertiary alkyl iodides 6 were used under similar conditions.",

author = "Liu, {Ju Tsung} and Yao, {Ching Fa}",

note = "Funding Information: Financial support of this work by the National Science Council of the Republic of China is gratefully acknowledged. ",

year = "2001",

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AU - Liu, Ju Tsung

AU - Yao, Ching Fa

N1 - Funding Information: Financial support of this work by the National Science Council of the Republic of China is gratefully acknowledged.

PY - 2001/8/27

Y1 - 2001/8/27

N2 - One-pot synthesis of (E)-alkenes 5 from the reactions of aldehyde 1 and nitromethane 2 in the acetic acid solution and then with triethylborane 4 in the biphase of diethyl ether and aqueous solution in the presence of oxygen in air was reported. Various (E)-alkenes 7 could also be prepared when different kinds of secondary or tertiary alkyl iodides 6 were used under similar conditions.

AB - One-pot synthesis of (E)-alkenes 5 from the reactions of aldehyde 1 and nitromethane 2 in the acetic acid solution and then with triethylborane 4 in the biphase of diethyl ether and aqueous solution in the presence of oxygen in air was reported. Various (E)-alkenes 7 could also be prepared when different kinds of secondary or tertiary alkyl iodides 6 were used under similar conditions.

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ER -

One-pot synthesis of trans-β-alkylstyrenes

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