An efficient and mild CuI/L-proline-catalyzed arylation of acetylacetone or ethyl cyanoacetate

Yongwen Jiang; Nan Wu; Haihong Wu; Mingyuan He

doi:10.1055/s-2005-918921

An efficient and mild CuI/L-proline-catalyzed arylation of acetylacetone or ethyl cyanoacetate

Yongwen Jiang^*
, Nan Wu
, Haihong Wu
, Mingyuan He

^*Corresponding author for this work

School of Chemistry and Molecular Engineering

East China Normal University

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

83 Scopus citations

Abstract

The coupling reaction of aryl iodides with acetylacetone or ethyl cyanoacetate under catalysis of CuI/L-proline works at relatively mild conditions to provide 3-aryl-2, 4-pentanediones and α-aryl cyanoacetates in moderate to good yields.

Original language	English
Article number	U24705ST
Pages (from-to)	2731-2734
Number of pages	4
Journal	Synlett
Issue number	18
DOIs	https://doi.org/10.1055/s-2005-918921
State	Published - 3 Nov 2005

Keywords

Additive
Aryl iodide
Arylation
Catalysis
Cross coupling

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10.1055/s-2005-918921

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@article{550331b995a64413b731d7d1f477a457,

title = "An efficient and mild CuI/L-proline-catalyzed arylation of acetylacetone or ethyl cyanoacetate",

abstract = "The coupling reaction of aryl iodides with acetylacetone or ethyl cyanoacetate under catalysis of CuI/L-proline works at relatively mild conditions to provide 3-aryl-2, 4-pentanediones and α-aryl cyanoacetates in moderate to good yields.",

keywords = "Additive, Aryl iodide, Arylation, Catalysis, Cross coupling",

author = "Yongwen Jiang and Nan Wu and Haihong Wu and Mingyuan He",

year = "2005",

month = nov,

day = "3",

doi = "10.1055/s-2005-918921",

language = "英语",

pages = "2731--2734",

journal = "Synlett",

issn = "0936-5214",

publisher = "Georg Thieme Verlag",

number = "18",

}

TY - JOUR

T1 - An efficient and mild CuI/L-proline-catalyzed arylation of acetylacetone or ethyl cyanoacetate

AU - Jiang, Yongwen

AU - Wu, Nan

AU - Wu, Haihong

AU - He, Mingyuan

PY - 2005/11/3

Y1 - 2005/11/3

N2 - The coupling reaction of aryl iodides with acetylacetone or ethyl cyanoacetate under catalysis of CuI/L-proline works at relatively mild conditions to provide 3-aryl-2, 4-pentanediones and α-aryl cyanoacetates in moderate to good yields.

AB - The coupling reaction of aryl iodides with acetylacetone or ethyl cyanoacetate under catalysis of CuI/L-proline works at relatively mild conditions to provide 3-aryl-2, 4-pentanediones and α-aryl cyanoacetates in moderate to good yields.

KW - Additive

KW - Aryl iodide

KW - Arylation

KW - Catalysis

KW - Cross coupling

UR - https://www.scopus.com/pages/publications/27844600643

U2 - 10.1055/s-2005-918921

DO - 10.1055/s-2005-918921

M3 - 文章

AN - SCOPUS:27844600643

SN - 0936-5214

SP - 2731

EP - 2734

JO - Synlett

JF - Synlett

IS - 18

M1 - U24705ST

ER -

An efficient and mild CuI/L-proline-catalyzed arylation of acetylacetone or ethyl cyanoacetate

Abstract

Keywords

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