Results 61 to 70 of about 1,246 (203)
Chiral Quaternary Ammonium Salt‐Catalyzed Enantioselective Addition Reactions of Hydantoins
Abstract We herein report a protocol for the asymmetric 1,4‐addition of hydantoins to various Michael acceptors by utilizing Cinchona alkaloid‐based chiral quaternary ammonium salt catalysts. Various products were obtained with moderate to good enantioselectivities and accompanying computational investigations helped to identify key interactions ...
Katharina Röser +5 more
wiley +1 more source
Heterocyclic organic compounds play pivotal roles in drug synthesis and continue to remain a fundamental area of research interest. The present study reports the synthesis, characterization and antibacterial activities of synthesized organic compounds ...
Tailor, Giriraj ; Department of Chemistry, Mewar University, Chittogarh, Rajasthan 312 901, India +4 more
core +2 more sources
Synthesis and crystal structure of (S)-5-isopropyl-5-methyl-2-thiohydantoin [PDF]
(S)-5-Isopropyl-5-methyl-2-thiohydantoin was synthesized by one-pot reaction of α-methyl-L-valine and thiourea in the absence of solvent. The crystal structure of this compound has been determined from single crystal X-ray diffraction data.
Fujinami, Shuhei +8 more
core +1 more source
Dopaminergic neuronal death via necroptosis in Parkinson's disease: A review of the literature
We reviewed the current literature on the potential role of necroptosis, a recently characterized regulated cell death mechanism, in Parkinson's disease (PD) pathogenesis. We summarized findings from studies on necroptosis in PD preclinical models and PD human tissue samples, discussing how manipulating necroptosis might open a novel therapeutic ...
Maria Regoni +2 more
wiley +1 more source
Fluorous parallel synthesis of a hydantoin/thiohydantoin library [PDF]
Fluorous tagging strategy is applied to solution-phase parallel synthesis of a library containing hydantoin and thiohydantoin analogs. Two perfluoroalkyl (Rf)-tagged alpha-amino esters each react with six aromatic aldehydes under reductive amination conditions. Twelve amino esters then each react with 10 isocyanates and isothiocyanates in parallel. The
Yimin, Lu, Wei, Zhang
openaire +2 more sources
Abstract Immunoisolation of pancreatic islets in alginate microcapsules allows for transplantation in the absence of immunosuppression but graft survival time is still limited. This limited graft survival is caused by a combination of tissue responses to the encapsulating biomaterial and islets. A significant loss of islet cells occurs in the immediate
Alexandra M. Smink +4 more
wiley +1 more source
Department of Chemistry, Sambalpur University, Sambalpur and Department of Chemistry, G. M. College, Sambalpur. Manuscript received 27 May 1972; accepted 4 July 1975. Several substituted benzothiazolyl thiohydantoias (I), their arylideae derivatives (II) and dibromo compounds (W) have been synthesised.
M. BEHERA, P. N. DHAL, A. NAYAK
openaire +2 more sources
The exposure systems of glycidol‐related chemicals on the formation of glycidol‐hemoglobin adducts diHOPrVal were compared. DiHOPrVal formation was observed using several chemicals other than glycidol with different behaviors in vitro and in vivo. However, in both cases, the amount of diHOPrVal produced was very small compared with glycidol. This study
Yuko Shimamura +4 more
wiley +1 more source
Solution-Phase Synthesis of a Combinatorial Thiohydantoin Library1
An efficient one-pot three-component synthesis of thiohydantoins was developed. In the first step, amino acid esters were alkylated by imine formation with aldehydes and reduction by sodium triacetoxyborohydride.
Mui Mui Sim (3030531) +1 more
core +2 more sources
Synthesis and molecular modeling studies of new thiohydantoin-triazole hybrids as anticancer agents
The targeted thiohydantoin-triazole hybrid compounds 5a-d and 9a-d were synthesized by the copper-catalyzed click reaction of 2-azido-N-arylacetamides 3a-d with the appropriate alkynes, thiohydantoin moiety linked to a propargyl group.
Wael M. Alamoudi
doaj +1 more source

