15017-21-7Relevant articles and documents
A highly selective colorimetric and fluorescent chemosensor for Al(III) based-on simple naphthol in aqueous solution
Liu, Zhaodi,Xu, Huajie,Sheng, Liangquan,Chen, Shuisheng,Huang, Deqian,Liu, Jie
, p. 6 - 10 (2016)
A colorimetric and fluorescent chemosensor (L) for Al(III) was synthesized and fully characterized. L could be both used as a colorimetric and fluorescent chemosensor for the detection of Al3 + ions with low detection limit (8.87 × 10- 7/
Antimicrobial activity of aroylhydrazone-based oxido vanadium(v) complexes: In vitro and in silico studies
Yousef Ebrahimipour,Sheikhshoaie, Iran,Simpson, Jim,Ebrahimnejad, Hadi,Dusek, Michal,Kharazmi, Nima,Eigner, Vaclav
, p. 2401 - 2412 (2016)
A tridentate Schiff base ligand (E)-N′-((2-hydroxynaphthalen-1-yl)methylene)benzohydrazide (H2L) and its oxido-vanadium(v) complexes with formulae [VO(L)(MeOH)(OMe)] (1), [VO(L)(OEt)] (2), and [VO(L)(OPr)] (3) have been synthesized and fully ch
Acylhydrazone Subunits as a Proton Cargo Delivery System in 7-Hydroxyquinoline
Antonov, Liudmil,Georgiev, Anton,Hirashima, Shin-ichi,Hori, Yutaro,Matsushima, Yasuyuki,Miura, Tsuyoshi,Nakashima, Kosuke,Petek, Anton,Yordanov, Dancho
, p. 11559 - 11566 (2021)
The reimagined concept of long-range tautomeric proton transfer using crane subunits is shown by designing and synthesising two new acylhydrazones containing a 7-hydroxyquinoline (7-OHQ) platform. The acylhydrazone subunits attached to the 7-OHQ at the 8t
Dioxido-vanadium(V) complex catalyzed oxidation of alcohols and tandem synthesis of oximes: a simple catalytic protocol for C–N bond formation
Kurbah, Sunshine Dominic
, p. 905 - 918 (2021/02/03)
We report the synthesis of a vanadium(V) complex characterized by FT-IR and 1H NMR spectroscopy. The structure of the complex was established by single crystal X-ray crystallography. We also carried out the catalytic oxidation of benzyl alcohol, hetero-aryl alcohols and propargylic alcohols. Tandem synthesis of oximes from alcohols were also carried out using our vanadium(V) complex. The newly synthesized complex acts as a catalyst for oxidation reactions and tandem synthesis of oxime from alcohols.
BF3-Etherate-catalyzed tandem reaction of 2-formylarylketones with electron-rich arenes/heteroarenes: An assembly of isobenzofurans
Mishra, Pawan K.,Kumar, Ankit,Verma, Akhilesh K.
supporting information, p. 6122 - 6125 (2020/06/18)
An efficient and BF3·Et2O-catalyzed chemoselective synthesis of diversified 1,3-diarylisobenzofuran in a high yield has been described. The reaction proceeds through sequential hydroarylation-cyclization between 2-formylarylketones and electron-rich arenes/heteroarenes. Advantageous features of the developed methodology include operational simplicity, a broad substrate scope, and applicability towards gram scale synthesis. The utility of isobenzofuran derivatives as the diene was extended to the synthesis of [4+2] cyclo-adducts with DMAD and the synthesis of 1,2-dicarbonylarenes in good yields.
