about
Synthesis, structure, and biological activity of des-side chain analogues of 1α,25-dihydroxyvitamin D3 with substituents at C18Design, synthesis, evaluation, and structure of vitamin D analogues with furan side chainsEquilibria between metallosupramolecular squares and triangles with the new rigid linker 1,4-bis(4-pyridyl)tetrafluorobenzene. Experimental and theoretical study of the structural dependence of NMR data.Clinical utility of simultaneous quantitation of 25-hydroxyvitamin D and 24,25-dihydroxyvitamin D by LC-MS/MS involving derivatization with DMEQ-TADPit-1 inhibits BRCA1 and sensitizes human breast tumors to cisplatin and vitamin D treatment.An efficient synthesis of 1α,25-dihydroxy-20-epi-vitamin D3.Synthesis of nonadeuterated 1α,25-dihydroxyvitamin D2.An efficient convergent synthesis of 1α,25-dihydroxy-3-epi-vitamin D2.26,26,26,27,27,27-Hexadeuterated-1,25-Dihydroxyvitamin D3 (1,25D-d6) As Adjuvant of Chemotherapy in Breast Cancer Cell Lines.Vitamin D receptor 2016: novel ligands and structural insights.Synthesis and biological evaluation of 1α,25-dihydroxyvitamin D₃ analogues with a long side chain at C12 and short C17 side chains.Carborane-based design of a potent vitamin D receptor agonist.A short practical approach to 24R,25-dihydroxyvitamin D3.A 4-hydroxypyrrolidine-catalyzed mannich reaction of aldehydes: control of anti-selectivity by hydrogen bonding assisted by Brønsted acids.X-ray diffraction, solution structure, and computational studies on derivatives of (3-sec-butyl-2,3-dihydro-1H-isoquinolin-4-ylidene)acetic acid: compounds with activity as calpain inhibitors.Synthesis, characterization, and magnetic properties of self-assembled compounds based on discrete homotrinuclear complexes of Cu(II).Evidence of desulfurization in the oxidative cyclization of thiosemicarbazones. Conversion to 1,3,4-oxadiazole derivatives.Synthesis and biological activity of the dihydrotachysterol2 metabolite 25-hydroxydihydrotachysterol2.New oxamato-bridged trinuclear Cu(II)-Cu(II)-Cu(II) complexes with hydrogen-bond supramolecular structures: synthesis and magneto-structural studies.A novel V(IV)O-pyrimidinone complex: synthesis, solution speciation and human serum protein binding.New oxamidato-bridged Cu(II)-Ni(II) complexes: supramolecular structures with thiocyanate ligands and hydrogen bonds. Magnetostructural studies: DFT calculations.Oxamato-bridged trinuclear NiIICuIINiII complexes: a new (NiIICuIINiII)2 hexanuclear complex and supramolecular structures. Characterization and magnetic properties.Magnetism of cyano-bridged hetero-one-dimensional Ln3+-M3+ complexes (Ln3+ = Sm, Gd, Yb; M3+ = FeLS, Co).PuPHOS: a synthetically useful chiral bidentate ligand for the intermolecular Pauson-Khand reaction.Base-dependent stereodivergent intramolecular aza-Michael reaction: asymmetric synthesis of 1,3-disubstituted isoindolines.Structure, magnetic properties and nuclease activity of pyridine-2-carbaldehyde thiosemicarbazonecopper(II) complexes.Magnetic properties of cyano-bridged Ln3+-M3+ complexes. Part I: trinuclear complexes (Ln3+ = La, Ce, Pr, Nd, Sm; M3+ = FeLS, Co) with bpy as blocking ligand.Magnetism of cyano-bridged Ln3+-M3+ complexes. Part II: one-dimensional complexes (Ln3+ = Eu, Tb, Dy, Ho, Er, Tm; M3+ = Fe or Co) with bpy as blocking ligand.Synthesis of highly condensed polycyclic carbohydrates by reaction of a spirocyclic enamino sulfonate derived from d-xylofuranose with bifunctional reagents.Boron trifluoride-induced, new stereospecific rearrangements of chiral epoxy ethers. Ready access to enantiopure 4-(diarylmethyl)-1,3-dioxolanes and 4,5-disubstituted tetrahydrobenzo[c]oxepin-4-ols.Self-assembly of ligands designed for the building of a new type of [2 x 2] metallic grid. anion encapsulation and diffusion NMR spectroscopy.Stereoselective Palladium-Catalyzed Approach to Vitamin D3 Derivatives in Protic Medium.Total synthesis of 1α,25-dihydroxyvitamin D3 (calcitriol) through a Si-assisted allylic substitution.1β,25-Dihydroxyvitamin D3: A new vitamin D metabolite in human serum.A new approach to 19-nor-A-ring phosphine oxide for the convergent synthesis of 19-nor-calcitriol.Phosphine-substrate recognition through the C-H...O hydrogen bond: application to the asymmetric Pauson-Khand reaction.Quantitative analytical method to evaluate the metabolism of vitamin D.Novel synthetic approach to 1alpha,25-dihydroxyvitamin D3 and analogues.Aromatic-Based Design of Highly Active and Noncalcemic Vitamin D Receptor AgonistsSynthesis, Crystal Structure, and Magnetic Studies of One-Dimensional Cyano-Bridged Ln3+−Cr3+Complexes with bpy as a Blocking Ligand
P50
Q27667567-7DE29818-DFD1-41BB-997F-DFA3118E9AD4Q27676147-20E7E003-D867-4B92-AC7D-2DC742BBF746Q30825006-E1702604-6ADC-42E6-9A55-E48A24F3F87FQ33837169-3BCB2CE9-1544-4588-A1F9-ACCEE79705C7Q35987385-98459D0F-C908-43DF-BCDC-4A9239347E95Q38080396-A76A9D01-AB43-4FD3-A9BA-8640834ADBBAQ38159897-19EC2180-5371-4EBC-9EFF-09430B889969Q38280521-25A63941-10E6-45A3-B673-0D59DE4D74ADQ38672183-FA1154E4-46DF-4FD2-A49C-D86D1149E5A1Q38907517-4ADAEA7F-4A38-4AD2-98B3-3897FAE0561CQ39276286-0DD9BC9E-7E7B-46A2-96E3-A4641ED7339CQ41150070-D6F8535C-2872-450C-8DFC-296A0EBD6A5AQ43102619-B9DD9CAD-6B52-43BD-8113-F1A18E12CB6AQ43121349-4F215C06-ED81-4F93-8B85-2C6C30D59290Q43218842-A44F5464-5781-42A2-BEA7-AC5644BF87B0Q43634798-BCFCCDC7-2233-4EAE-9BF2-65084A59A819Q43919186-0B88E76D-BA52-442D-89EF-627799F98715Q43993745-80EDB966-BCC5-4481-B6BE-748797966403Q44177514-FF920B2E-EB9C-45F2-BE2F-F2B4358F17A2Q44206373-232B6CD7-662A-4DF6-AB49-B47C6C400AF1Q44241291-44286177-6733-4FE4-978B-B22D64E8DA8BQ44436096-ECC1CA46-AC1A-4C6B-B01D-9C79F266DC7FQ44553183-F93C7609-3E93-4CEF-99BC-5DDDADB80397Q45139817-04AD4F66-0060-4107-96C9-7A277CF5F17DQ46022631-31BDBBCE-65CF-445D-B5B0-DC727B5477ACQ46436224-100BE06D-8911-4DCF-99A5-3D00040DCCCEQ46717830-0DC505CF-59D4-452B-B0F7-1AEB10C0512FQ46717836-B1FB8C68-7CB6-4EBF-A6FB-F54DF01F2168Q46902346-17859FD6-B883-48AC-ABEF-24969A68F506Q46936383-99B0D750-2E9E-4A56-AD0F-0521FA33184CQ46971207-DD6A6C74-EBE1-4876-995A-B2F43E934087Q48119150-DE257371-8656-49E0-A44B-5294FDC55299Q48731987-5047592A-5F06-4FCD-BB60-7E93FA323641Q50895459-1D8291CD-DE0A-4CFE-96A9-CC35AB6BB51BQ52856901-18256B60-E81C-4519-96F2-D79BC8A2DFA9Q52992942-79DFBB4A-C1CB-4A14-A315-6FFDE9FFF6DBQ53241311-CFA6C8B9-AD77-41D7-BF5D-C42ECE25C819Q54601796-455F8AEA-05CE-444B-B8A5-E0ACE0494866Q60891182-CB9F8038-BC3B-4E34-AA1E-788E83A50770Q63888445-D96901D6-A6EE-43A8-9F3B-6824385650AD
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Miguel Maestro
@ast
Miguel Maestro
@en
Miguel Maestro
@es
Miguel Maestro
@nl
Miguel Maestro
@sl
type
label
Miguel Maestro
@ast
Miguel Maestro
@en
Miguel Maestro
@es
Miguel Maestro
@nl
Miguel Maestro
@sl
prefLabel
Miguel Maestro
@ast
Miguel Maestro
@en
Miguel Maestro
@es
Miguel Maestro
@nl
Miguel Maestro
@sl
P1053
H-5194-2015
P106
P1153
35956482900
P21
P2798
P31
P3829
P3835
miguel-maestro
P496
0000-0001-8922-8033