Electrochemical Synthesis of trans-Olefins from Buta-1,3-dienes and Alkyl Halides

Haoxiang Zhang; Lin Guo; Chao Yang; Wujiong Xia

doi:10.1055/a-2006-1285

Electrochemical Synthesis of trans-Olefins from Buta-1,3-dienes and Alkyl Halides

Haoxiang Zhang
, Lin Guo
, Chao Yang^*
, Wujiong Xia^*

^*Corresponding author for this work

Harbin Institute of Technology
Henan Normal University

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

4 Scopus citations

Abstract

A facile electrochemical alkylation reaction of buta-1,3-diene derivatives with alkyl halides has been developed, generating highly selective trans-olefins as major products. This method exhibits significant advantages, including simple operation, mild conditions, and convenience of scale-up, and provides a novel route for the synthesis of trans-olefins.

Original language	English
Pages (from-to)	3033-3039
Number of pages	7
Journal	Synthesis (Germany)
Volume	55
Issue number	18
DOIs	https://doi.org/10.1055/a-2006-1285
State	Published - 29 Aug 2023
Externally published	Yes

Keywords

1
3-dienes
alkyl halides
electrochemical reduction
radicals
trans-olefins

Access to Document

10.1055/a-2006-1285

Cite this

@article{0ef697bbe71b4751ba96c7cbe1ebcc8b,

title = "Electrochemical Synthesis of trans-Olefins from Buta-1,3-dienes and Alkyl Halides",

abstract = "A facile electrochemical alkylation reaction of buta-1,3-diene derivatives with alkyl halides has been developed, generating highly selective trans-olefins as major products. This method exhibits significant advantages, including simple operation, mild conditions, and convenience of scale-up, and provides a novel route for the synthesis of trans-olefins.",

keywords = "1, 3-dienes, alkyl halides, electrochemical reduction, radicals, trans-olefins",

author = "Haoxiang Zhang and Lin Guo and Chao Yang and Wujiong Xia",

year = "2023",

month = aug,

day = "29",

doi = "10.1055/a-2006-1285",

language = "英语",

volume = "55",

pages = "3033--3039",

journal = "Synthesis (Germany)",

issn = "0039-7881",

publisher = "Georg Thieme Verlag",

number = "18",

}

TY - JOUR

T1 - Electrochemical Synthesis of trans-Olefins from Buta-1,3-dienes and Alkyl Halides

AU - Zhang, Haoxiang

AU - Guo, Lin

AU - Yang, Chao

AU - Xia, Wujiong

PY - 2023/8/29

Y1 - 2023/8/29

N2 - A facile electrochemical alkylation reaction of buta-1,3-diene derivatives with alkyl halides has been developed, generating highly selective trans-olefins as major products. This method exhibits significant advantages, including simple operation, mild conditions, and convenience of scale-up, and provides a novel route for the synthesis of trans-olefins.

AB - A facile electrochemical alkylation reaction of buta-1,3-diene derivatives with alkyl halides has been developed, generating highly selective trans-olefins as major products. This method exhibits significant advantages, including simple operation, mild conditions, and convenience of scale-up, and provides a novel route for the synthesis of trans-olefins.

KW - 1

KW - 3-dienes

KW - alkyl halides

KW - electrochemical reduction

KW - radicals

KW - trans-olefins

UR - https://www.scopus.com/pages/publications/85146806698

U2 - 10.1055/a-2006-1285

DO - 10.1055/a-2006-1285

M3 - 文章

AN - SCOPUS:85146806698

SN - 0039-7881

VL - 55

SP - 3033

EP - 3039

JO - Synthesis (Germany)

JF - Synthesis (Germany)

IS - 18

ER -

Electrochemical Synthesis of trans-Olefins from Buta-1,3-dienes and Alkyl Halides

Abstract

Keywords

Access to Document

Other files and links

Fingerprint

Cite this