82645-24-7Relevant articles and documents
Spectroscopic and electrochemical studies of transition metal complexes with N,N′-bis(2-aminothiophenol)-1,7-bis(2-formylphenyl)-1,4,7- trioxaheptane and structure effects on extractability of ligand towards some divalent cations
Temel, Hamdi,Alp, Hueseyin,Ilhan, Salih,ZiyadanogullarI, Berrin,YIlmaz, Ismail
, p. 1199 - 1209 (2007)
La(III), Cu(II), Ni(II), and Zn(II) metal complexes with a novel quadridentate Schiff base derived from 1,7-bis(2-formylphenyl)-1,4,7- trioxaheptane and 2-aminothiophenol were synthesized and characterized by microanalytical data, elemental analysis, magn
Formation of a four-bladed waterwheel-type chloro-bridged dicopper(ii) complex with dithiamacrocycle: Via double exo-coordination
Kim, Seulgi,Park, In-Hyeok,Choi, Han-Byeol,Ju, Huiyeong,Lee, Eunji,Herng, Tun Seng,Ding, Jun,Jung, Jong Hwa,Lee, Shim Sung
supporting information, p. 1365 - 1369 (2020/02/15)
A combination of O3S2-macrocycles incorporating different sulfur-to-sulfur separations (S-(CH2)n-S, L1: N = 2, L2: N = 3) and copper(ii) nitrate afforded new types of both monocopper(ii) an
DIMER COMPOUNDS, AND USE IN BINDING TOXIC REPEATS OF RNA
-
Paragraph 0230; 0231, (2020/07/16)
Provided herein are compounds and methods for modulating abnormal repeat expansions of gene sequences. More particularly, provided are dimeric inhibitors of RNA and the uses of such inhibitors in regulating nucleotide repeat expansions, e.g., to treat Myotonic Dystrophy Type 1 (DM1), Myotonic Dystrophy Type 2 (DM2), Fuchs dystrophy, Huntington Disease, Amyotrophic Lateral Sclerosis, or Frontotemporal Dementia.
Exploitation of Intramolecular Glaser-Eglinton-Hay Macrocyclization for the Synthesis of New Classes of Optically Active Aza-Oxo-Thia Polyether Macrocycles from Amino Alcohol Building Blocks
Babu, Srinivasarao Arulananda
supporting information, p. 253 - 259 (2017/01/25)
We report an intramolecular Glaser-Eglinton-Hay coupling as an unprecedented route for assembling optically active aza-oxo polyether macrocycles containing a 1,3-diyne unit from enantiopure amino alcohol building blocks and suitable linkers. Furthermore, the conversion of the 1,3-diyne unit of the aza-oxo polyether macrocycles into a thiophene ring led to the assembly of new classes of optically active aza-oxa-thia (heterotopic) polyether macrocycle analogues of classical 18-C-6 and 18-C-5 systems.