Ionic liquid-accelerated N-arylation of benzoazoles with diaryliodonium salts, an efficient method for the synthesis of N-aryl azoles

Feng-Yan Wang; Zhen-Chu Chen; Qinguo Zheng

doi:10.3184/0308234041640690

Ionic liquid-accelerated N-arylation of benzoazoles with diaryliodonium salts, an efficient method for the synthesis of N-aryl azoles

Feng-Yan Wang, Zhen-Chu Chen, Qinguo Zheng

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

Abstract

N-Arylation of benzoazoles with diaryliodonium salts can be performed in good yields in the room-temperature ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate ([bmim]BF4), which provides an efficient method for the synthesis of N-arylbenzoazoles. The ionic liquid can be recycled and reused.

Original language	English
Pages (from-to)	206-207
Number of pages	2
Journal	Journal of Chemical Research
Volume	2004
Issue number	3
DOIs	https://doi.org/10.3184/0308234041640690
Publication status	Published - Mar 2004

Keywords

ionic liquids
indoles
benzimidazoles
diaryliodonium salts
N-arylation of azoles

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10.3184/0308234041640690

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title = "Ionic liquid-accelerated N-arylation of benzoazoles with diaryliodonium salts, an efficient method for the synthesis of N-aryl azoles",

abstract = "N-Arylation of benzoazoles with diaryliodonium salts can be performed in good yields in the room-temperature ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate ([bmim]BF4), which provides an efficient method for the synthesis of N-arylbenzoazoles. The ionic liquid can be recycled and reused.",

keywords = "ionic liquids, indoles, benzimidazoles, diaryliodonium salts, N-arylation of azoles",

author = "Feng-Yan Wang and Zhen-Chu Chen and Qinguo Zheng",

year = "2004",

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doi = "10.3184/0308234041640690",

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pages = "206--207",

journal = "Journal of Chemical Research",

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T1 - Ionic liquid-accelerated N-arylation of benzoazoles with diaryliodonium salts, an efficient method for the synthesis of N-aryl azoles

AU - Wang, Feng-Yan

AU - Chen, Zhen-Chu

AU - Zheng, Qinguo

PY - 2004/3

Y1 - 2004/3

N2 - N-Arylation of benzoazoles with diaryliodonium salts can be performed in good yields in the room-temperature ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate ([bmim]BF4), which provides an efficient method for the synthesis of N-arylbenzoazoles. The ionic liquid can be recycled and reused.

AB - N-Arylation of benzoazoles with diaryliodonium salts can be performed in good yields in the room-temperature ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate ([bmim]BF4), which provides an efficient method for the synthesis of N-arylbenzoazoles. The ionic liquid can be recycled and reused.

KW - ionic liquids

KW - indoles

KW - benzimidazoles

KW - diaryliodonium salts

KW - N-arylation of azoles

UR - http://www.scopus.com/inward/record.url?scp=2942620207&partnerID=8YFLogxK

UR - https://journals.sagepub.com/doi/abs/10.3184/0308234041640690

U2 - 10.3184/0308234041640690

DO - 10.3184/0308234041640690

M3 - Article

SN - 0308-2342

VL - 2004

SP - 206

EP - 207

JO - Journal of Chemical Research

JF - Journal of Chemical Research

IS - 3

ER -

Ionic liquid-accelerated N-arylation of benzoazoles with diaryliodonium salts, an efficient method for the synthesis of N-aryl azoles

Abstract

Keywords

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