Results 141 to 150 of about 2,171 (198)

Comparative Genomic and Transcriptomic Analysis Reveals Why Paenarthrobacter Strains Are Specialists in the Degradation of the Fungicide Iprodione. [PDF]

Microb Biotechnol
Michelioudakis V, Zafranas A, Myrisiotis C, Makri S, Katsoula A, Campos M, Vasileiadis S, Karpouzas DG.   +7 more
europepmc   +1 more source

A promising dual catalytic "Isothiourea + X" platform: from classic ionic to radical transformations. [PDF]

RSC Adv
Zhang B, Li Y, Ji Z, Wang J.
europepmc   +1 more source

Poly(methyl vinyl ether-<i>alt</i>-maleic anhydride) and Its Derivatives: From Polymer Synthesis to Advanced Biomedical Applications. [PDF]

Polymers (Basel)
Badía-Hernández PV, Díaz-Puertas R, Sánchez-García PDC, Falcó A, García-Morales P, Mallavia R.   +5 more
europepmc   +1 more source

Combinatorial chemistry of hydantoins

Bioorganic & Medicinal Chemistry Letters, 1998
Access to combinatorial chemistry of hydantoins is provided by convenient and versatile methods for the solid phase synthesis of libraries of 3,5-, 1,3- and 1,3,5-substituted hydantoins. The preparation of trisubstituted hydantoins features a Mitsunobu reaction for introduction of the substituent on N-1.
Boeijen, A., Kruijtzer, J.A.W., Liskamp, R.M.J.   +2 more
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The Chemistry of the Hydantoins.

Chemical Reviews, 1950
exaly   +3 more sources

A Sustainable, Semi‐Continuous Flow Synthesis of Hydantoins

Chemistry - A European Journal, 2016
Hydantoins are an important class of heterocycles with applications in pharmacy, agriculture, and as intermediates in organic synthesis. Traditional synthetic procedures to access hydantoins are target oriented with multiple synthetic steps, often use ...
Kerry Gilmore, Beate Koksch, Peter Seeberger   +2 more
exaly   +2 more sources

Facile synthesis of hydantoins and thiohydantoins in aqueous solution

Tetrahedron Letters, 2011
A series of hydantoins and thiohydantoins have been synthesized in water at room temperature from urea (or N-methylurea, or thiourea) and simple aldehydes (as glyoxal, and its simple derivatives) in the presence of phosphoric anhydride. The reaction time
Gabriele Micheletti, Camilla Delpivo, Boga Carla   +2 more
exaly   +2 more sources

Microchemical tests for hydantoins and barbiturate-hydantoin mixtures

Microchemical Journal, 1972
Abstract Substituted hydantoins, a number of which possess anticonvulsant activity and are prescribed alone or compounded with barbiturates, were observed to enter into a number of reactions commonly utilized to identify barbituric acid derivatives. The reactivity of the hydantoins with the Dille-Koppanyi and the Zwikker tests is sufficiently similar
Edward F. Rhodes, John I. Thornton
openaire   +1 more source

SELENIUM-CONTAINING HYDANTOINS

Phosphorus and Sulfur and the Related Elements, 1988
Abstract The influence of the exo-chalcogen atoms on the hydantoin skeleton of the complete series of molecules NH C(=X) NH C(=Y)CMe2 (X, Y = O, S, Se) has been studied from several points of view.
F. A. Devillanova, ISAIA, FRANCESCO, G. Verani   +2 more
openaire   +2 more sources

Hydantoins as antitumor agents

Journal of Medicinal Chemistry, 1977
A series of 27 hydantoins was prepared and tested as antitumor agents. These were variously substituted in the 5 position but with special emphasis on the substituents (chloro, acetyl, chloroacetyl, and methyl) in the 1 and/or 3 positions. The most active compound was 5,5-bis(4-chlorophenyl)-1,3-dichlorohydantoin with a T/C value of 190% against P-388 ...
T R, Rodgers, M P, LaMontagne, A, Markovac, A B, Ash   +3 more
openaire   +2 more sources