The Experts below are selected from a list of 11853 Experts worldwide ranked by ideXlab platform
Baohua Chen - One of the best experts on this subject based on the ideXlab platform.
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one pot synthesis of 4 substituted 1h 1 2 3 triazolo 4 5 c quinolines through cuo promoted tandem cyclization reactions of e 3 2 bromoaryl 1 arylprop 2 en 1 ones with Sodium Azide
ChemInform, 2014Co-Authors: Jinying Chen, Yongxin Chen, Xin Guo, Chunxia Chen, Baohua ChenAbstract:Copper-promoted tandem cyclization of 2-bromoarylenones of type (I) with Sodium Azide offers a direct synthesis of triazoloquinolines (II).
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one pot synthesis of 2 4 5 trisubstituted 1 2 3 triazoles through the cascade reactions of acid chlorides terminal acetylenes Sodium Azide and aryl halides
New Journal of Chemistry, 2013Co-Authors: Xiang Liu, Baohua ChenAbstract:An efficient one-pot reaction of acid chlorides, terminal acetylenes, Sodium Azide and aryl halides is developed for the regioselective synthesis of 2,4,5-trisubstituted 1,2,3-triazoles. The method is general, convenient, eco-friendly, atom-economical, and could provide excellent yields and regioselectivities.
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one pot synthesis of 4 5 disubstituted 1 2 3 nh triazoles using terminal acetylenes carbon monoxide aryl iodides and Sodium Azide
Tetrahedron Letters, 2011Co-Authors: Dong Wang, Weilin Shi, Baohua ChenAbstract:Abstract A one-pot method for the synthesis of 4,5-disubstituted-1,2,3-(NH)-triazoles via carbonylative Sonogashira reaction / 1,3-dipolar cycloaddition of terminal acetylenes, carbon monoxide, aryl iodides, and Sodium Azide was developed. A series of new 4,5-disubstituted-1,2,3-(NH)-triazoles were prepared readily under mild conditions.
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facile one pot synthesis of 4 5 disubstituted 1 2 3 nh triazoles through sonogashira coupling 1 3 dipolar cycloaddition of acid chlorides terminal acetylenes and Sodium Azide
Organic Letters, 2009Co-Authors: Dong Wang, Yuanqing Zhang, Baohua ChenAbstract:A novel and efficient way of synthesizing 4,5-disubstituted-1,2,3-(NH)-triazoles through palladium-catalyzed and ultrasonic promoted Sonogashira coupling/1,3-dipolar cycloaddition of acid chlorides, terminal acetylenes, and Sodium Azide in one pot is developed. The reaction scope is quite general, and the methodology can produce excellent yields. The regioselective 1,4,5-trisubstituted-1,2,3-(NH)-triazoles can be made easily from 4,5-disubstituted-1,2,3-(NH)-triazoles.
Dong Wang - One of the best experts on this subject based on the ideXlab platform.
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one pot synthesis of 4 5 disubstituted 1 2 3 nh triazoles using terminal acetylenes carbon monoxide aryl iodides and Sodium Azide
Tetrahedron Letters, 2011Co-Authors: Dong Wang, Weilin Shi, Baohua ChenAbstract:Abstract A one-pot method for the synthesis of 4,5-disubstituted-1,2,3-(NH)-triazoles via carbonylative Sonogashira reaction / 1,3-dipolar cycloaddition of terminal acetylenes, carbon monoxide, aryl iodides, and Sodium Azide was developed. A series of new 4,5-disubstituted-1,2,3-(NH)-triazoles were prepared readily under mild conditions.
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facile one pot synthesis of 4 5 disubstituted 1 2 3 nh triazoles through sonogashira coupling 1 3 dipolar cycloaddition of acid chlorides terminal acetylenes and Sodium Azide
Organic Letters, 2009Co-Authors: Dong Wang, Yuanqing Zhang, Baohua ChenAbstract:A novel and efficient way of synthesizing 4,5-disubstituted-1,2,3-(NH)-triazoles through palladium-catalyzed and ultrasonic promoted Sonogashira coupling/1,3-dipolar cycloaddition of acid chlorides, terminal acetylenes, and Sodium Azide in one pot is developed. The reaction scope is quite general, and the methodology can produce excellent yields. The regioselective 1,4,5-trisubstituted-1,2,3-(NH)-triazoles can be made easily from 4,5-disubstituted-1,2,3-(NH)-triazoles.
Yinghong Zhu - One of the best experts on this subject based on the ideXlab platform.
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Copper-Catalyzed Tandem Reactions of 2-Iodobenzamides with Sodium Azide: An Efficient Synthesis of [1,2,3]Triazolo[1,5-a][1,4]-benzodiazepin-6(5H)-ones.
ChemInform, 2015Co-Authors: Wanli Chen, Yinghong ZhuAbstract:The title compounds are efficiently obtained by reaction of 2-iodobenzamides with a propargyl group on the nitrogen atom moiety and Sodium Azide under mild reaction conditions.
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Copper-Catalyzed Tandem Reactions of 2-Iodobenzamides with Sodium Azide: An Efficient Synthesis of [1,2,3]Triazolo[1,5-a][1,4]-benzodiazepin-6(5H)-ones
Synlett, 2015Co-Authors: Wanli Chen, Yinghong ZhuAbstract:Copper-catalyzed tandem reactions between 2-iodobenzamides with a propargyl group on the nitrogen atom moiety and Sodium Azide are presented, providing an efficient method for the synthesis of 3-substituted [1,2,3]triazolo[1,5- a ][1,4]benzodiazepin-6(5 H )-ones under mild conditions in moderate yields.
Qing Yang - One of the best experts on this subject based on the ideXlab platform.
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copper catalyzed synthesis of 4 aryl 1h 1 2 3 triazoles from 1 1 dibromoalkenes and Sodium Azide
European Journal of Organic Chemistry, 2012Co-Authors: Xiaokun Wang, Chunxiang Kuang, Qing YangAbstract:A new methodology for the Cu-catalyzed synthesis of 1H-1,2,3-triazoles from 1,1-dibromoalkenes and Sodium Azide is presented. Aryl dibromoolefins were efficiently converted into the corresponding 1,2,3-triazoles. A comprehensive number of functional groups were compatible with this reaction. 1,2,3-Triazoles were obtained in moderate to excellent yields.
Yunfeng Chen - One of the best experts on this subject based on the ideXlab platform.
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aluminium iii chloride catalyzed three component condensation of aromatic aldehydes nitroalkanes and Sodium Azide for the synthesis of 4 aryl nh 1 2 3 triazoles
Advanced Synthesis & Catalysis, 2016Co-Authors: Qinquan Hu, Xiaocong Deng, Yanjun Li, Yunfeng ChenAbstract:An aluminium(III) chloride-catalyzed three-component reaction of aromatic aldehydes, nitroalkanes, and Sodium Azide has been developed; this reaction sequence can be applied to a broad substrate scope and affords the corresponding 4-aryl-NH-1,2,3-triazoles in good to excellent yields. The milder reaction conditions and easier operation make this AlCl3-catalyzed protocol more advantageous for the synthesis of 4-aryl-NH-1,2,3-triazoles.
