4467-90-7Relevant academic research and scientific papers
An efficient method for the synthesis of α-arylated nitroalkanes and α-arylated hydroximoyl chlorides mediated by AlCl3
Tu, Zhijay,Rama Raju,Liou, Tzuo-Rung,Kavala, Veerababurao,Kuo, Chun-Wei,Jang, Yaochung,Shih, Yu-Hsuan,Wang, Chun-Chao,Yao, Ching-Fa
experimental part, p. 2436 - 2442 (2009/07/25)
Friedel-Crafts alkylation of various arenes/heteroarenes to β-nitrostyrenes mediated by aluminum chloride is described. The interesting feature of this methodology pertain the formation of different products by tuning the reaction temperature. α-Arylated
Synthesis of isoxazole conjugates of 1,4-benzodioxane moiety via intermolecular 1,3-dipolar cycloaddition
Vaidya, Vipraja V.,Wankhede, Karuna S.,Nara, Susheel J.,Salunkhe, Manikrao M.,Trivedi, Girish K.
body text, p. 3856 - 3866 (2009/12/08)
1,3-Dipolar cycloaddition was utilized as a tool to conjugate the 1,4-benzodioxane moiety with several biologically active compounds such as steroid, sugar, and other aromatic scaffolds via isoxazole or triazole bridge. The propynyl ether of 2-hydroxymethyl-1,4-benzodioxane underwent 1,3-dipolar cycloadditions smoothly with different in situ generated nitrile oxides in good yields. The triazole conjugate of 1,4-benzodioxane was synthesized via click chemistry. Copyright Taylor & Francis Group, LLC.
A facile one-pot preparation of isothiocyanates from aldoximes
Kim, Jae Nyoung,Jung, Keum Shin,Lee, Hong Jung,Son, Ji Suk
, p. 1597 - 1598 (2007/10/03)
Isothiocyanates 2a-l were prepared in excellent yields in a one-pot reaction from aldoxime derivatives 1a-l by successive treatment of aldoxime with N-chlorosuccinimide (NCS), thiourea, and triethylamine. The use of HCl/DMF/Oxone system in the reaction instead of NCS was equally effective.
