Results 101 to 110 of about 20,280 (253)

Correction to: Azo group(s) in selected macrocyclic compounds. [PDF]

J Incl Phenom Macrocycl Chem, 2018
Wagner-Wysiecka E, Łukasik N, Biernat JF, Luboch E.   +3 more
europepmc   +1 more source

Dioxygen Reduction at a Cu(I) Complex Supported by a Macrocyclic N3O Ligand System

Chemistry – A European Journal, EarlyView.
A non‐reactive [CuI(14‐TMC)]+ complex is transformed to an efficient catalyst [CuI(14‐TMCO)]+ (TMCO = 4,8,12‐trimethyl‐1‐oxa‐4,8,12‐triazacyclotetradecane) for 4e−/4H+ reduction of O2 by N → O substitution. ABSTRACT CuI(14 TMCO) (1), involving a N3O‐macrocycle, reacts with O2 at cryogenic temperatures to yield an end‐on peroxodicopper(II) species.
Maximilian Schütze, Dibya Jyoti Barman, Christian Lorent, Kallol Ray   +3 more
wiley   +1 more source

Two-Step Synthesis of Complex Artificial Macrocyclic Compounds. [PDF]

Angew Chem Int Ed Engl, 2017
Madhavachary R, Abdelraheem EMM, Rossetti A, Twarda-Clapa A, Musielak B, Kurpiewska K, Kalinowska-Tłuścik J, Holak TA, Dömling A.   +8 more
europepmc   +1 more source

Synthesis, Physicochemical Characteristics, Self‐Assembly and Encapsulation Ability of per‐Ethylene‐Glycol‐Functionalized Resorcin[4]Arenes and Their Molecular Capsules: On the Road to Liquid Capsules

Chemistry – A European Journal, EarlyView.
Per‐ethylene‐glycol (EG)‐functionalized resorcin[4]arenes containing 12, 16, and 20 EG groups namely compounds 1d, 1e, and 1f, respectively, were prepared and found to self‐assemble, in organic solvents, into hexameric capsules. These capsules are more dynamic than the ones prepared based on alkyl substituted resorcin[4]arenes.
Gangadhara Angajala, Inbar Horin, Tamar Evan‐Salem, Yoram Cohen   +3 more
wiley   +1 more source

Novel Macrocyclic Compounds Targeting STING for Autoimmune Diseases Treatment. [PDF]

ACS Med Chem Lett
Jiang Y, Liang SH.
europepmc   +1 more source

Thiol-to-amine cyclization reaction enables screening of large libraries of macrocyclic compounds and the generation of sub-kilodalton ligands. [PDF]

Sci Adv, 2019
Kale SS, Bergeron-Brlek M, Wu Y, Kumar MG, Pham MV, Bortoli J, Vesin J, Kong XD, Machado JF, Deyle K, Gonschorek P, Turcatti G, Cendron L, Angelini A, Heinis C.   +14 more
europepmc   +1 more source

From Caffeine to Aspirin: Everyday Molecules as Triggers for Genetically Encoded Proximity Systems

Chemistry – A European Journal, EarlyView.
This Perspective article highlights how familiar dietary ingredients and over‐the‐counter (OTC) drugs (such as caffeine and its metabolites, SA, and aspirin) can be repurposed as clinically translatable chemical triggers for genetically encoded proximity systems.
Mingguang Cui, Tianlu Wang, Yaoyu Han, Yun Huang, Tien‐Hung Lan, Yunbin Zhou   +5 more
wiley   +1 more source

Thio-modified trianglimines, a novel group of chiral macrocyclic compounds of high structural dynamics. [PDF]

Sci Rep
Prusinowska N, Czapik A, Szymkowiak J, Kwit M.   +3 more
europepmc   +1 more source

Lanthanide Centered and Circular Polarized Luminescence (CPL) From Tb(III) Complexes Made From Structurally Simple Methoxy‐Phenyl and Phenol‐Derived Pyridyldiamide (pda) Ligands

Chemistry – A European Journal, EarlyView.
The development of chiral pda derived methoxy ligands L1a [1(R,R)] and L1b [1(S,S)], along with their phenol derivatives L2a [2(R,R)] and L2b [2(S,S)], and their respective Tb(III) complexes is described. These Tb‐complexes exhibited Tb(III)‐centered emission upon and their chiroptical properties were probed by using both CD and CPL spectroscopy ...
Jennifer E. Jones, Jonathan A. Kitchen, Robert D. Peacock, Thorfinnur Gunnlaugsson   +3 more
wiley   +1 more source

Validating Small-Molecule Force Fields for Macrocyclic Compounds Using NMR Data in Different Solvents. [PDF]

J Chem Inf Model
Waibl F, Casagrande F, Dey F, Riniker S.
europepmc   +1 more source