about
Three-component reaction of tautomeric amidines with 3-ferrocenylmethylidene-2,4-pentanedione. Formation of polymeric coordination complexes of potassium ferrocenyl-(hexahydro)pyrimidoxides.Diosgenin hemihydrate.The mitochondrial apoptotic pathway is induced by Cu(II) antineoplastic compounds (Casiopeínas®) in SK-N-SH neuroblastoma cells after short exposure times.Enrofloxacin hydro-chloride dihydrate.Potential cytotoxic and amoebicide activity of first row transition metal compounds with 2,9-bis-(2',5'-diazahexanyl)-1,1-phenanthroline (L1).Cytotoxic copper(II), cobalt(II), zinc(II), and nickel(II) coordination compounds of clotrimazole.[1,2-Bis(diisopropyl-phosphan-yl)ethane-κ(2) P,P'](carbonato-κ(2) O,O')nickel(II).Water-Soluble Ruthenium (II) Chiral Heteroleptic Complexes with Amoebicidal in Vitro and in Vivo Activity.Side-on cupric-superoxo triplet complexes as competent agents for H-abstraction relevant to the active site of PHM.Aqua-[1,8-bis-(pyridin-2-yl)-3,6-dithia-octane-κN,S,S',N']copper(II) dinitrate acetonitrile monosolvate.N-crotylphthalimide.2-(1,3-Thia-zol-4-yl)benzimidazolium nitrate monohydrate.Crystal structure of (E)-1-(2-nitro-benzyl-idene)-2,2-di-phenyl-hydrazine.exo-1,7-Dimethyl-4-phenyl-10-oxa-4-aza-tri-cyclo-[5.2.1.0(2,6)]dec-8-ene-3,5-dione.5-Chloro-2-methyl-sulfanyl-6-(naphtha-len-1-yl-oxy)-1H-benzimidazole methanol monosolvate.(E)-1,1-Diphenyl-2-(thio-phen-2-yl-methyl-idene)hydrazine.(E)-1-(2,4-Di-nitro-benzyl-idene)-2,2-di-phenyl-hydrazine.1,3-Bis[(-)-(S)-(1-phenyl-eth-yl)imino-meth-yl]benzene.Diosgenone: a second P2(1) polymorphTris(5,6-dimethyl-1,10-phenanthroline-κ(2)N,N')copper(II) bis-(hexa-fluorido-phosphate) acetonitrile monosolvate.(R)-3,3-Diethyl-1-(2-hy-droxy-1-phenyl-eth-yl)piperidin-2-one.(E)-1-(3,4-Dimethyl-benzyl-idene)-2,2-diphenyl-hydrazine.5-Fluoro-1-[(4S,5R)-5-(2-hydroxy-ethyl)-2,2-dimethyl-1,3-dioxolan-4-yl]pyrimidine-2,4(1H,3H)-dione.(E)-1-(4-Nitro-benzyl-idene)-2,2-diphenyl-hydrazineCrystal structure of ethyl 3-anilino-2-{[bis-(methyl-sulfan-yl)methyl-idene]amino}-3-oxopropano-ate.Crystal structure of 1-mesityl-3-methyl-4-phenyl-1H-1,2,3-triazol-3-ium iodide.Crystal structure of the chalcone (E)-3-(furan-2-yl)-1-phenylprop-2-en-1-one.Intramolecular transformations of 3-cyanoamino- and 3-cyanoimino-1,2-diferrocenylcyclopropenes.High-field EPR study and crystal and molecular structure of trans-RSSR-[CrCl2(cyclam)]nX (X=ZnCl4 2-, Cl- and Cl-.4H2O.0.5HCl).Diacetoxyiodobenzene-mediated synthesis of unnatural furospirostane sapogenins derived from diosgenin and tigogenin.Mechanistic insights on the reactivity of furospirostanes with the 16β,22:22,25-diepoxy-23-acetoxymethyl-24-methyl side chain.Synthesis of 24-phenyl-24-oxo steroids derived from bile acids by palladium-catalyzed cross coupling with phenylboronic acid. NMR characterization and X-ray structures.Effect of tunable redox behavior of bis chelate substituted 1,10-phenantroline Cu(II) complexes on its reaction with superoxide anion in DMSO. Toward a simple criterion to identify a SOD-like mechanism.A family of rhodium and iridium complexes with semirigid benzylsilyl phosphines: from bidentate to tetradentate coordination modes.Hypervalent-iodine induced quasi-Favorskii C-ring contraction of 12-oxosteroids: a shortcut to C-norsteroids.Supramolecular fluorescence enhancement via coordination-driven self-assembly in bis-picolylcalixarene blue-emitting M2L2Xn macrocycles.4-Ferrocenylpyridine- and 4-ferrocenyl-3-ferrocenylmethyl-3,4-dihydropyridine-3,5-dicarbonitriles: multi-component synthesis, structures and electrochemistry.Baeyer-Villiger reaction of steroid sapogenins by CF3COOH-H2O2. A short cut to pregnan-3β,16β,20-triol 3-monoacetates.Transformations in Chemically Responsive Copper-Calixarene Architectures.Coumarin Derivative Directly Coordinated to Lanthanides Acts as an Excellent Antenna for UV-Vis and Near-IR Emission.
P50
Q30722712-C4540C21-F524-4FB0-9489-E5279CD1A31DQ36148872-E111844A-D52A-4EEA-B756-C23F0F7EABBDQ38725601-53ED98F9-6A43-4AC9-B1E3-5A44CBAB60B3Q38948686-3AD221A7-F3A8-4F01-8BD3-877FD450E011Q39327176-539B9BB8-6701-4A2A-AA41-DDC43027B3FCQ39327850-86E99C9B-5707-4E1C-A8A4-7A59FE9EDF85Q39923887-49538DE4-20FB-48F4-8075-9C7C25F84D50Q40376750-0798B55A-9257-49CD-8E6D-18BBD563DD55Q40837027-BFB2BE44-4955-4061-A632-0FD5109D1746Q40932528-EB43CDAA-1301-4B6B-BAE4-4F1CD9E2CB5DQ41518796-7AA2780E-013D-4230-BA2C-A629563A0690Q41840294-1D33D13B-1167-4AD6-8D9F-999B15323324Q41855680-1CAA99CA-DA61-4225-B3EE-03275F72D634Q41859243-839E52FD-1A72-48D4-A00D-76032E837A8EQ41914756-8CDAD42A-3A1D-42C7-A8F4-3C1521D30C78Q41914763-B2A5162F-B1FF-4BFF-ACCB-5AE2F3A865FEQ41977928-70BD61E9-74F8-4ABC-A75A-0E9D83F81A29Q42021150-4C2467C3-13EC-464F-BB5D-8EB434C1B56BQ42174684-8E8C514B-8528-48EB-8826-753B3F384D15Q42231155-2997DEF5-CC71-45FB-B118-C16E60EB87EEQ42266357-27BFADB7-F41C-4FBD-8BD6-D0399411289BQ42275089-4A0B248A-0BA6-4A43-B649-63EEEDB428D6Q42368145-2BE37DFB-DD7C-4E54-86F0-D8E55BD5C653Q42390668-947DCDA5-6D3A-4EDE-9FFF-7CBB5C303381Q42930342-8D9CE7A8-D4F3-4925-B225-110A4ACA2520Q43078152-42EC0402-B5AA-440E-AF63-393CCD455002Q43215995-16830B2A-E8C1-4102-94EE-2348BE090FB4Q43270568-A3B6B473-713A-4D6D-BC06-1A79441595B7Q45012856-5DCECE20-8043-4E62-8513-69498A7B9321Q45330548-367882DA-AC3B-423C-AB3C-97AEA672218CQ46160873-F04CC4D1-304E-47FA-B4A3-6FA89C122E91Q46267332-78254140-79B9-45F5-938D-869FB0886787Q46329289-4276BD70-8A74-4A0C-B721-8E37C1B8F0A2Q46388458-0BAC7F6F-190D-4522-A5A7-DF773FE05A51Q46408071-4736B0BA-05C5-49CF-89A4-D83673DCD79AQ46683329-47D5E9E5-51F7-4ABD-9E9B-EEBAB47BC6B3Q47222968-F99E49E3-63C9-40B5-B051-52C014E16FE8Q47811114-F9E5C653-28FB-4A11-8339-FE342FE05A67Q48279046-0F1E7F64-E582-4E57-B7D6-71C5094E6E11Q48296617-1A370F80-4EEF-414B-BC38-E6BED0EF564B
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description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Marcos Flores-Alamo
@ast
Marcos Flores-Alamo
@en
Marcos Flores-Alamo
@es
Marcos Flores-Alamo
@nl
type
label
Marcos Flores-Alamo
@ast
Marcos Flores-Alamo
@en
Marcos Flores-Alamo
@es
Marcos Flores-Alamo
@nl
prefLabel
Marcos Flores-Alamo
@ast
Marcos Flores-Alamo
@en
Marcos Flores-Alamo
@es
Marcos Flores-Alamo
@nl
P106
P1153
56000774300
P21
P31
P496
0000-0002-2996-7616