94830-76-9Relevant academic research and scientific papers
Design and Development of Axially Chiral Bis(naphthofuran) Luminogens as Fluorescent Probes for Cell Imaging
Jejurkar, Valmik P.,Yashwantrao, Gauravi,Kumar, Pawan,Neekhra, Suditi,Maliekal, Parimal J.,Badani, Purav,Srivastava, Rohit,Saha, Satyajit
, p. 5470 - 5482 (2021)
Designing chiral AIEgens without aggregation-induced emission (AIE)-active molecules externally tagged to the chiral scaffold remains a long-standing challenge for the scientific community. The inherent aggregation-caused quenching phenomenon associated w
Synthesis and antifungal activities of some aryl naphthofuran ketoximes
Karaburun, Ahmet Cagri,Gundogdu-Karaburun, Nalan,Ucucu, Umit,Demirayak, Seref
experimental part, p. 758 - 762 (2012/05/05)
In this study, some aryl naphtho[2, 1-b]furan-2-yl ketoximes and their ethers and esters were synthesised. The structure elucidation of the compounds was performed by IR, 1H-NMR and MASS spectroscopic data and elemental analyses results. Antifungal activities of the compounds were tested against Candida albicans (two strains), Candida glabrata, Candida tropicalis and Candida parapsilosis using a microbroth dilution technique. The results showed that the compounds displayed minimum inhibitory concentrations, 7.8-625 μg/mL.
An expedient synthesis of enantioenriched substituted (2-benzofuryl) arylcarbinols via tandem Rap-Stoermer and asymmetric transfer hydrogenation reactions
Kumaraswamy, Gullapalli,Ramakrishna, Gajula,Raju, Ragam,Padmaja, Mogilisetti
experimental part, p. 9814 - 9818 (2011/02/22)
An expedient synthesis of enantioenriched substituted (benzofuran-yl)-aryl and heteroaryl carbinols, is described. A key feature of this protocol is synthesis of functionally varied benzofuran scaffolds via a Rap-Stoermer reaction/catalytic asymmetric tra
Microwave-mediated solvent free Rap-Stoermer reaction for efficient synthesis of benzofurans
Rao, Maddali L.N.,Awasthi, Dheeraj K.,Banerjee, Debasis
, p. 431 - 434 (2008/02/03)
The Rap-Stoermer reaction of salicylaldehydes with diverse phenacyl bromide and phenacyl iodides proceeded cleanly to afford various functionalized benzofurans in excellent yields under base-mediated solvent free microwave irradiation conditions.
Synthesis and cytotoxic evaluation of α-methylene-γ-butyrolactone bearing naphthalene and naphtho[2,1-b]furan derivatives
Lee, Kuan-Han,Huang, Bor-Ruey
, p. 333 - 338 (2007/10/03)
Naphthalene α-methylene-γ-butyrolactones exhibits a unique cytotoxicity profile. They are highly cytostatic for leukaemia cancer cells but are not cytocidal. For almost all the solid tumours tested, they are both cytostatic and cytocidal. Substitution of a bromo atom on either naphthalene or both naphthalene and γ-phenyl moiety of the lactone enhanced potency while retaining the same cytotoxicity profile. The tricyclic naphtho[2,1-b]furan derivatives, prepared from 2-hydroxy-1-naphthaldehyde in an efficient pathway, also possess the same cytotoxicity profile.
Novel Copper(II)-mediated Photocyclization of Methoxynaphthyl Analogues of Chalcone: Unusual Electron Transfer from Excited Vinyl Arenes
Kar, Samiran,Lahiri, Saswati
, p. 957 - 958 (2007/10/02)
Copper(II)-mediated photocyclization of the title compounds to naphthofurans via an electron-transfer process is reported.
