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^*

^*Corresponding author for this work

Department of Chemistry

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

45 Citations (Scopus)

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.

Original language	English
Pages (from-to)	6147-6150
Number of pages	4
Journal	Tetrahedron Letters
Volume	42
Issue number	35
DOIs	https://doi.org/10.1016/S0040-4039(01)01185-6
Publication status	Published - 2001 Aug 27

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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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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doi = "10.1016/S0040-4039(01)01185-6",

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T1 - One-pot synthesis of trans-β-alkylstyrenes

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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UR - https://www.scopus.com/pages/publications/0035959474#tab=citedBy

U2 - 10.1016/S0040-4039(01)01185-6

DO - 10.1016/S0040-4039(01)01185-6

M3 - Article

AN - SCOPUS:0035959474

SN - 0040-4039

VL - 42

SP - 6147

EP - 6150

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 35

ER -

One-pot synthesis of trans-β-alkylstyrenes

Abstract

ASJC Scopus subject areas

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