Convenient method for the preparation of 2-aryl-1H-benzimidazole-4-carboxylic acids

J Cheng; NY Xiu; XB Li; XJ Luo

doi:10.1080/00397910500188942

Convenient method for the preparation of 2-aryl-1H-benzimidazole-4-carboxylic acids

J Cheng, NY Xiu, XB Li, XJ Luo^*

^*Corresponding author for this work

Chemistry

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

9 Citations (Scopus)

Abstract

The oxidative cyclization of 2,3-diaminobenzoic acid and aromatic aldehydes to give 2-aryl-1H-benzimidazole-4-carboxylic acids is reported. Moreover, three methods were compared in different perspectives from experimental manipulation to yield.

Original language	English
Pages (from-to)	2395-2399
Number of pages	5
Journal	Synthetic communications
Volume	35
Issue number	18
DOIs	https://doi.org/10.1080/00397910500188942
Publication status	Published - 2005

Keywords

benzimidazole
pharmaceutical synthesis
potassium ferricyanide
RESISTANCE-MODIFYING AGENTS
POLY(ADP-RIBOSE) POLYMERASE
INHIBITORS
REPAIR

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10.1080/00397910500188942

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title = "Convenient method for the preparation of 2-aryl-1H-benzimidazole-4-carboxylic acids",

abstract = "The oxidative cyclization of 2,3-diaminobenzoic acid and aromatic aldehydes to give 2-aryl-1H-benzimidazole-4-carboxylic acids is reported. Moreover, three methods were compared in different perspectives from experimental manipulation to yield.",

keywords = "benzimidazole, pharmaceutical synthesis, potassium ferricyanide, RESISTANCE-MODIFYING AGENTS, POLY(ADP-RIBOSE) POLYMERASE, INHIBITORS, REPAIR",

author = "J Cheng and NY Xiu and XB Li and XJ Luo",

year = "2005",

doi = "10.1080/00397910500188942",

language = "English",

volume = "35",

pages = "2395--2399",

journal = "Synthetic communications",

issn = "0039-7911",

publisher = "Taylor and Francis Ltd.",

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TY - JOUR

T1 - Convenient method for the preparation of 2-aryl-1H-benzimidazole-4-carboxylic acids

AU - Cheng, J

AU - Xiu, NY

AU - Li, XB

AU - Luo, XJ

PY - 2005

Y1 - 2005

N2 - The oxidative cyclization of 2,3-diaminobenzoic acid and aromatic aldehydes to give 2-aryl-1H-benzimidazole-4-carboxylic acids is reported. Moreover, three methods were compared in different perspectives from experimental manipulation to yield.

AB - The oxidative cyclization of 2,3-diaminobenzoic acid and aromatic aldehydes to give 2-aryl-1H-benzimidazole-4-carboxylic acids is reported. Moreover, three methods were compared in different perspectives from experimental manipulation to yield.

KW - benzimidazole

KW - pharmaceutical synthesis

KW - potassium ferricyanide

KW - RESISTANCE-MODIFYING AGENTS

KW - POLY(ADP-RIBOSE) POLYMERASE

KW - INHIBITORS

KW - REPAIR

U2 - 10.1080/00397910500188942

DO - 10.1080/00397910500188942

M3 - Article

SN - 0039-7911

VL - 35

SP - 2395

EP - 2399

JO - Synthetic communications

JF - Synthetic communications

IS - 18

ER -

Convenient method for the preparation of 2-aryl-1H-benzimidazole-4-carboxylic acids

Abstract

Keywords

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