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A Convenient Synthesis of 2-Arylnaphtho[1,2-d]oxazole Derivatives Promoted by Triethylamine
引用本文:李红 韦堃 吴养洁. A Convenient Synthesis of 2-Arylnaphtho[1,2-d]oxazole Derivatives Promoted by Triethylamine[J]. 中国化学, 2007, 25(11): 1704-1709. DOI: 10.1002/cjoc.200790315
作者姓名:李红 韦堃 吴养洁
作者单位:Henan Key Laboratory of Chemical Biology and Organic Chemistry, and Key Laboratory of Applied Chemistry of Henan Universities, Department of Chemistry, Zhengzhou University, Zhengzhou, Henan 450052, China
基金项目:Project supported by the National Natural Science Foundation of China (No. 20472074) and the Innovation found for 0utstanding Scholars of Henan Province (No. 0621001100).
摘    要:A variety of 2-arylnaphtho[ 1,2-d]oxazole derivatives were efficiently synthesized in moderate to high yields by the reaction of aromatic aldehydes with 1-amino-2-naphthol derivatives in the presence of triethylamine in refluxing ethanol in air. Seven new 2-arylnaphtho[1,2-d]oxazole derivatives were obtained and characterized by the spectral data and elemental analysis. In addition, the X-ray crystal structures of 2-[4-(N,N-dimethylamino)phenyl]naphtho[ 1,2-d] oxzole (3d) and 1, 1'-bis(naphtho[ 1,2-d]oxazol-2-yl)ferrocene (3n) have been determined.

关 键 词:1  3-氧氮杂茂 芳族胺 1-胺基-2-萘酚 三乙烷基 晶体结构
修稿时间:2007-02-02

A Convenient Synthesis of 2-Arylnaphtho[1,2-d]oxazole Derivatives Promoted by Triethylamine
LI, Hong WEI, Kun WU, Yang-Jie. A Convenient Synthesis of 2-Arylnaphtho[1,2-d]oxazole Derivatives Promoted by Triethylamine[J]. Chinese Journal of Chemistry, 2007, 25(11): 1704-1709. DOI: 10.1002/cjoc.200790315
Authors:LI   Hong WEI   Kun WU   Yang-Jie
Affiliation:Henan Key Laboratory of Chemical Biology and Organic Chemistry, and Key Laboratory of Applied Chemistry of Henan Universities, Department of Chemistry, Zhengzhou University, Zhengzhou, Henan 450052, China
Abstract:A variety of 2-arylnaphtho[1,2-d]oxazole derivatives were efficiently synthesized in moderate to high yields by the reaction of aromatic aldehydes with 1-amino-2-naphthol derivatives in the presence of triethylamine in refluxing ethanol in air. Seven new 2-arylnaphtho[1,2-d]oxazole derivatives were obtained and characterized by the spectral data and elemental analysis. In addition, the X-ray crystal structures of 2-[4-(N,N-dimethylamino)phenyl]naphtho[1,2-d] oxzole ( 3d ) and 1,1′-bis(naphtho[1,2-d]oxazol-2-yl)ferrocene ( 3n ) have been determined.
Keywords:2-arylnaphtho[1  2-d]oxazole   1-amino-2-naphthol derivative   triethylamine   crystal structure
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