Results 51 to 60 of about 106,351 (226)
2-C-Cyclohexyl-2,3-O-isopropylideneerythrofuranose
In the title compound, C13H22O4, the acetonide ring adopts an envelope conformation with one of the O atoms as the flap atom, whereas a twisted conformation is found for the furanose ring.
Edward R. T. Tiekink +2 more
doaj +1 more source
Supramolecular Thermo Aero-able Gelators (STAGs) for synthesis of hydrogels
Supramolecular Thermo Aero-able Gelators (STAGs): tartaric acid, urea, and guanidine with amide and imine moieties as supramolecular synthons are introduced to cross-link and aerate ('aero-able') polyacrylate networks for synthesis of hydrogels. They are
Atharva Sahasrabudhe +8 more
core +1 more source
Crystal structure of the N-benzyloxycarbonyl-Alanyl-Phenylalanyl-methyl ester: the importance of the H-bonding pattern [PDF]
Large crystals of the methyl ester of the N-a-benzyloxycarbonyl protected Ala-Phe dipeptide (Z-AF-OMe) were obtained after the very slow evaporation of a solution of the corresponding carboxylic acid (Z-AF-OH) in methanol containing an excess of HCl. The
Alfonso, Ignacio +3 more
core +2 more sources
Structural studies of crystalline forms of triamterene with carboxylic acid, GRAS and API molecules. [PDF]
Pharmaceutical salt solvates (dimethyl sulfoxide, DMSO) of the drug triamterene with the coformers acetic, succinic, adipic, pimelic, azelaic and nicotinic acid and ibuprofen are prepared by liquid-assisted grinding and solvent-evaporative ...
Delori, Amit +3 more
core +2 more sources
Is there any point in making co-crystals? [PDF]
Citation: Aakeroy, C. (2015). Is there any point in making co-crystals? Acta Crystallographica Section B-Structural Science Crystal Engineering and Materials, 71, 387-391.
Aakeröy, Christer B.
core +1 more source
Harnessing hydrogen-bonding: advancements and applications in pharmaceutical co-crystallization
Background: In the context of supramolecular chemistry, the formation of solid-state structures that exhibit predictable form and function through the use of intermolecular interactions is known as crystal engineering.
Preeti Devi +4 more
doaj +1 more source
(2,2′-Bipyridyl)bis[N,N-bis(2-hydroxyethyl)dithiocarbamato-κ2S,S′]cadmium(II)
The title compound, [Cd(C5H10NO2S2)2(C10H8N2)], features a trigonal-prismatic coordination geometry for the CdII ion, based on an N2S4 donor set defined by two chelating dithiocarbamate ligands and a 2,2′-bipyridyl ligand.
Edward R. T. Tiekink, Juyoung C. Song
doaj +1 more source
Supramolecular synthons, tectons, and crystal structures of noncovalent organic frameworks
In reticular chemistry, framework structures formed from organic molecules by noncovalent intermolecular interactions [i.e., noncovalent organic frameworks (nCOFs)] have been intensively investigated over the last two decades as another type of candidate
I. Hisaki, Takuto Fujii, R. Oketani
semanticscholar +1 more source
Intermolecular interactions, in particular hydrogen bonds, play a key role in crystal engineering. The ability to form hydrogen bonds of various types and strengths causes competition between supramolecular synthons in pharmaceutical multicomponent ...
Alexander P. Voronin +3 more
doaj +1 more source
A one‐pot protocol to synthesize reactive benzyl‐ and allyl‐halide‐substituted (dihydro)naphthalenes from 2,3‐aryl‐1,3‐butadiene substrates and halogenated alkanes has been developed, using [Cp*RuCl(PPh3)2] as the catalyst. Mechanistic studies revealed an atom transfer radical addition and radical benzannulation sequence, followed by HCl elimination ...
Nicole S. van Leeuwen +9 more
wiley +1 more source

