One-Pot Synthesis of 1-(E)-Phenylethenyl-1,2,3-Triazoles by Sequential Click-Elimination Reaction from 2-Azido-1-Phenyl-1-(Phenylseleno)Ethane-Reference-Cited by-同舟云学术

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One-Pot Synthesis of 1-(E)-Phenylethenyl-1,2,3-Triazoles by Sequential Click-Elimination Reaction from 2-Azido-1-Phenyl-1-(Phenylseleno)Ethane

Published:2013-09-20 Issue:11 Volume:188 Page:1591-1598
ISSN:1042-6507
Container-title:Phosphorus, Sulfur, and Silicon and the Related Elements
language:en
Short-container-title:Phosphorus, Sulfur, and Silicon and the Related Elements

Author:

Su Hai-You¹,Sheng Shou-Ri²,Zhang Xiao-Lan³,Ding Xiao-Ying¹,Cai Ming-Zhong¹

Affiliation:

1. a Institutes of Chemistry and Chemical Engineering , Jiangxi Normal University , Nanchang , P.R. China

2. b Key Laboratory of Functional Small Organic Molecule, Ministry of Education , Jiangxi Normal University , Nanchang , P.R. China

3. c Department of Chemistry , Shangrao Normal College , Shangrao , P.R. China

Publisher

Informa UK Limited

Subject

Inorganic Chemistry,Organic Chemistry,Biochemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/10426507.2013.769987

Reference36 articles.

1. 1,2,3-Triazoles and their Benzo Derivatives

2. Substituent Effects on the Antibacterial Activity of Nitrogen−Carbon-Linked (Azolylphenyl)oxazolidinones with Expanded Activity Against the Fastidious Gram-Negative Organisms Haemophilus influenzae and Moraxella catarrhalis

3. Studies on 1,2,3-triazoles. 13. (Piperazinylalkoxy)-[1]benzopyrano[2,3-d]-1,2,3-triazol-9(1H)-ones with combined H1-antihistamine and mast cell stabilizing properties

4. 1,2,3-Triazole-[2,5-Bis-O-(tert-butyldimethylsilyl)-.beta.-D-ribofuranosyl]-3'-spiro-5''-(4''-amino-1'',2''-oxathiole 2'',2''-dioxide) (TSAO) Analogs: Synthesis and Anti-HIV-1 Activity

5. The Synthesis of Triazole Analogues of Antitumor Dehydropyrrolizidine Alkaloids

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1. Polystyrene resin supported palladium(0) (Pd@PR) nanocomposite mediated regioselective synthesis of 4-aryl-1-alkyl/(2-haloalkyl)-1H-1,2,3-triazoles and their N-vinyl triazole derivatives from terminal alkynes;RSC Advances;2015

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