Results 71 to 80 of about 697 (188)

Synthesis of Thiohydantoin-Castanospermine Glycomimetics as Glycosidase Inhibitors

open access: yesThe Journal of Organic Chemistry, 2009
The preparation of bicyclic carbohydrate mimics related to (+)-castanospermine incorporating a thiohydantoin moiety is reported. The synthetic approach is compatible with molecular diversity-oriented strategies and involves alpha-azidoesters, built at the C-5/C-6 segment in gluco- or galactofuranose scaffolds, as the key precursors.
Aguilar Moncayo, Matilde   +3 more
openaire   +3 more sources

Synthesis and characterization of a methacrylate monomer with a thiohydantoin structure

open access: yesJournal of Oral Science, 2020
The purpose of the current study was to synthesize a methacrylate monomer with a thiohydantoin structure. In a flask, (2-thiohydantoin-4-yl) propionic acid, 10-hyroxydecyl methacrylate, 4-dimethylaminopyridine, and tetrahydrofuran (THF) were placed in a nitrogen atmosphere.
Matsumura, Hideo   +5 more
openaire   +3 more sources

Proton magnetic resonance study of the conformation of the pyrrolidine ring in some proline-thiohydantoins

open access: yes, 1988
The conformational behaviour of a series of N-substituted thiohydantoins of proline was studied by proton NMR. The pseudorotational parameters of the proline moiety were calculated from the ten vicinal proton-proton coupling constants assuming a two ...
Marc J. O. Anteunis   +5 more
core   +1 more source

Density Functional Theory Guided Design of Exo-Selective Dehydroalanine Dienophiles for Application Toward the Synthesis of Palau'amine

open access: yes, 2016
Diels−Alder cycloadditions of dehydroalanine derivatives with cyclopentadiene, applicable to the synthesis of palau'amine, were investigated experimentally and using DFT computations at the B3LYP/6-31G* level of theory.
James L. Gleason (1853971)   +1 more
core   +2 more sources

Synthesis of 3-substituted 5-arylidene-1-methyl-2-thiohydantoins under microwave irradiation

open access: yes, 2002
A mono-modal microwave oven was used to expedite the synthesis of small libraries of 3-substituted 1-methyl-2-thiohydantoins and 3-substituted 5-arylidene-1-methyl-2-thiohydantoins.
Nielsen, John   +2 more
core  

Conventional and microwave-assisted synthesis of 1,5-diaryl-2-thiohydantoins

open access: yes, 2012
891-894A simple and efficient method for synthesis of new 1,5-diaryl-2-thiohydantoins using microwave radiation has been standardized. The compounds have been synthesized from phenyl¬acetic acid by esterification, bromination, amination and cyclization ...
Baile, M B, Mahajan, S S
core  

Substituted 5,5'-diphenyl-2-thioxoimidazolidin-4-one as CB1 cannabinoid receptor ligands: synthesis and pharmacological evaluation.

open access: yes, 2005
A set of 30 substituted 5,5'-diphenyl-2-thioxoimidazolidin-4-one (thiohydantoins) derivatives was synthesized, and their affinity for the human CB(1) cannabinoid receptor has been evaluated.
Wouters, Johan   +10 more
core   +1 more source

Kinetics and mechanism of racemisation reactions of configurationally labile stereogenic centres in drug-like molecules in aqueous solutions; thiohydantoins and related compounds [PDF]

open access: yes
In this thesis, studies of the kinetic and mechanism of racemisation of several drug-like molecule have been presented. Chapter 1 provides background information on the general mechanisms of racemisation of drugs in general, and hydantoin derivatives. In
Ahmad, Hiwa Omer
core  

Substituted 5,5‘-Diphenyl-2-thioxoimidazolidin-4-one as CB1 Cannabinoid Receptor Ligands:  Synthesis and Pharmacological Evaluation

open access: yes, 2016
A set of 30 substituted 5,5‘-diphenyl-2-thioxoimidazolidin-4-one (thiohydantoins) derivatives was synthesized, and their affinity for the human CB1 cannabinoid receptor has been evaluated.
Jacques H. Poupaert (2069590)   +6 more
core   +1 more source

It is “2-imino-4-thiazolidinones” and not thiohydantoins as the reaction product of 1,3-disubstituted thioureas and chloroacetylchloride

open access: yes, 2008
The products obtained by the reaction of 1,3-disubstituted thioureas with chloroacetylchloride are actually 2-imino-4-thiazolidinone derivatives and not thiohydantoins as previously reported (M. Kidwai, R. Venkataraman and B. Dave, Green. Chem., 2001, 3,
Ghosh, Harisadhan   +2 more
core   +1 more source

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