about
New anacardic acid-inspired benzamides: histone lysine acetyltransferase activators.Substitution Effects of Hypervalent Iodine(III) Reagents in the Diamination of Styrene.Synthesis and biological characterization of the histone deacetylase inhibitor largazole and C7- modified analogues.Competing thermal electrocyclic ring-closure reactions of (2Z)-hexa-2,4,5-trienals and their Schiff bases. Structural, kinetic, and computational studies.Synthesis of benzamides related to anacardic acid and their histone acetyltransferase (HAT) inhibitory activities.Sigmatropic Rearrangement of Vinyl Aziridines: Expedient Synthesis of Cyclic Sulfoximines from Chiral Sulfinimines.Machines vs Malaria: A Flow-Based Preparation of the Drug Candidate OZ439Development of a flow method for the hydroboration/oxidation of olefinsDFT Rationalization of the Diverse Outcomes of the Iodine(III)-Mediated Oxidative Amination of AlkenesPseudopericyclic design drives antara-antara [1,5] methylene sigmatropic shifts from a stepwise to a concerted mechanism2-Alkylidenesulfol-3-enes by (regio- and) stereoselective cheletropic addition of SO2 to (di)vinylallenesIodine(III)-promoted intermolecular diamination of alkenesIodine(III)-mediated intermolecular allylic amination under metal-free conditionsMetal-free iodine(III)-promoted direct intermolecular C-H amination reactions of acetylenesEnantioselective metal-free diamination of styrenesHypervalent iodine mediated oxidative amination of allenesIsolation of stable non cyclic 1,2-disulfoxides. Revisiting the thermolysis of S-aryl sulfiniminesDefined hypervalent iodine(III) reagents incorporating transferable nitrogen groups: nucleophilic amination through electrophilic activationOxidative diamination promoted by dinuclear iodine(III) reagentsIndole synthesis based on a modified Koser reagent
P50
Q39671625-E4EF3A8A-6494-4232-A6FE-CA62E24A0BADQ39678343-D60F0E1C-6576-496A-94CE-20AB7EB8DCC4Q39701630-6C3EC10F-4AC7-4CA8-A7AD-1A571B95E1AAQ43045282-7B4A2B27-FE8F-45F9-B74E-F8C8FDA8F61DQ46553505-C3E28A71-483C-432F-A868-9BBD463C27C3Q48162500-6EA67680-8F3A-4935-B9A2-F096D35D4B4CQ56747854-933B7B73-BF75-4326-9D73-46987A38F00AQ56951476-5876CD38-7128-4948-998E-D7D7F52BE784Q58830878-2E5EB02C-CD9F-4B79-AC22-5828FB3DACCAQ79852123-2B68E9CF-360F-48BC-A958-6AE2996BE228Q81625987-00BE9FE5-0076-49C1-B437-6A8DA0AAD862Q83555441-BA224C07-D53C-4B8E-95FF-C694B9B85C6CQ83900694-E117BADA-A0C1-42CC-9CB7-918A43790B7DQ84836106-28F07C7C-5F85-4A7D-A0CA-ACE3E69ACD36Q84988918-693DDADF-C6FC-4CD7-B7EA-1BAE4E6B0CC0Q85250557-B3C2C202-B498-4ABF-942B-335B1AB3AE2BQ85287560-AB7ABAFC-8329-4B03-9A57-CECC05EDC56BQ85603806-CE468808-FB67-4957-BB1F-3F8C45D87002Q86100352-590E34D8-B087-4D53-8653-2225F6609DFDQ88008731-D22149E6-7093-41DB-B129-AB5D444CBE5A
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
José A Souto
@ast
José A Souto
@en
José A Souto
@es
José A Souto
@nl
José A Souto
@sl
type
label
José A Souto
@ast
José A Souto
@en
José A Souto
@es
José A Souto
@nl
José A Souto
@sl
prefLabel
José A Souto
@ast
José A Souto
@en
José A Souto
@es
José A Souto
@nl
José A Souto
@sl
P1053
A-1324-2017
P106
P21
P2456
P31
P3829
P3835
jose-souto4
P496
0000-0001-9138-8220