about
Water as the reaction medium for multicomponent reactions based on boronic acidsBoronic Acids and Esters in the Petasis-Borono Mannich Multicomponent ReactionAxial coordination of NHC ligands on dirhodium(II) complexes: generation of a new family of catalysts.Tetra-mu-acetato-bis{[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]rhodium(II)}(Rh-Rh) tetrahydrofuran tetrasolvate.Recyclable stereoselective catalysts.Making expensive dirhodium(II) catalysts cheaper: Rh(II) recycling methods.Homologation Reaction of Ketones with Diazo Compounds.Reversible lysine modification on proteins by using functionalized boronic acids.Glycerol as an efficient medium for the petasis borono-mannich reaction.Targeting cancer cells with folic acid-iminoboronate fluorescent conjugates.Electronic and Functional Scope of Boronic Acid Derived Salicylidenehydrazone (BASHY) Complexes as Fluorescent Dyes.Site-selective installation of BASHY fluorescent dyes to Annexin V for targeted detection of apoptotic cells.Modular Assembly of Reversible Multivalent Cancer-Cell-Targeting Drug Conjugates.Corrigendum: Reversible Lysine Modification on Proteins by Using Functionalized Boronic Acids.Chimeric Small Antibody Fragments as Strategy to Deliver Therapeutic Payloads.Improved thermostable polyvinyl alcohol electrospun nanofibers with entangled naringinase used in a novel mini-packed bed reactor.Studies on the Preparation of 4-Ethoxyalkyliden and 4-Aminoalkyliden-5(4H)-oxazolonesDiazaborines as New Inhibitors of Human Neutrophil ElastaseConstruction of homogeneous antibody-drug conjugates using site-selective protein chemistryIminoboronates are efficient intermediates for selective, rapid and reversible -terminal cysteine functionalisationCysteine-Selective Reactions for Antibody ConjugationDiscovery of new heterocycles with activity against human neutrophile elastase based on a boron promoted one-pot assembly reactionN-Heterocyclic Carbene Catalyzed Addition of Aldehydes to Diazo Compounds: Stereoselective Synthesis of N-AcylhydrazonesRing-Expansion Reaction of Isatins with Ethyl Diazoacetate Catalyzed by Dirhodium(II)/DBU Metal-Organic System: En Route to Viridicatin AlkaloidsAsymmetric Intramolecular CH Insertion of α-Diazoacetamides in Water by Dirhodium(II) Catalysts Derived from Natural Amino AcidsFour-Component Assembly of Chiral N–B Heterocycles with a Natural Product-Like FrameworkIminoboronates: A New Strategy for Reversible Protein ModificationNHC/Iron cooperative catalysis: aerobic oxidative esterification of aldehydes with phenolsα-Rhamnosidase and β-glucosidase expressed by naringinase immobilized on new ionic liquid sol–gel matrices: Activity and stability studiesNHC−Iron-Catalyzed Aerobic Oxidative Aromatic Esterification of Aldehydes using Boronic AcidsNew dirhodium complex with activity towards colorectal cancerSelective arylation of aldehydes with di-rhodium(II)/NHC catalystsEfficient catalyst reuse by simple dissolution in non-conventional mediaTuning the Reactivity of Dirhodium(II) Complexes with Axial N-Heterocyclic Carbene Ligands: The Arylation of AldehydesRh(II)-Catalyzed Intramolecular C−H Insertion of Diazo Substrates in Water: Scope and LimitationsSimple transformation of crystalline chiral natural anions to liquid medium and their use to induce chiralityRh(ii) catalysed intramolecular C–H insertion of diazo substrates in water: a simple and efficient approach to catalyst reuseN,O-Iminoboronates: Reversible Iminoboronates with Improved Stability for Cancer Cells Targeted DeliveryBioconjugation with Maleimides: A Useful Tool for Chemical BiologySequence Programming with Dynamic Boronic Acid/Catechol Binary Codes
P50
Q29541226-C8C86C8C-3494-4780-8C7E-997B7C724FE2Q30053332-5BE73C63-D20D-4D60-90F7-DE97ECA83357Q31154450-DD1CCEA8-8C3C-4175-AF9A-6B4A35548F60Q33374257-B99CDC76-1969-4C87-951C-BF5B9DB07B26Q37390581-CB7B4083-B879-4587-8121-CEDD96A5DB81Q37994587-D14FC1D4-2F46-4751-9511-D5FEC6480B14Q38725903-4D34033E-6170-4893-92D9-AE5F7703CB0DQ38883755-B5F5D67B-F3A7-4266-8728-C503AB9E7CB3Q42093992-C6EE060E-A971-4598-A6F6-372A148EAC04Q44588616-10C7B9B2-8639-4782-8745-46F50ADEA7FFQ48144527-767C79EC-9B1B-453D-B72F-EC3B8933AB69Q48170821-139B0A64-C8BC-4C9C-873F-001B4EC936C9Q48306721-FDE27866-BC4A-470E-9813-9DD47D6D5FA0Q51313527-7F897372-A6F5-4DBA-A132-98F9D2291F59Q52313534-A0C2F383-3F5F-4013-BE8D-C3E48BCBC06AQ53135949-C11EC25A-6E8B-4F6D-93BE-26C6111174EFQ57634165-D9D54B26-89F9-4025-A9D8-579BB4CEC640Q57976114-C71CA335-885F-49A3-9E7F-DFAECAEBD982Q57976132-999A95A4-E6D2-4AE9-8218-06706B26345DQ57976137-79313B92-F5BD-4F8F-AC6B-4144FC735DBCQ57976145-5FF0372D-50B5-4B1B-A67E-4EABDE1A7E5FQ57976161-CCB210CD-7483-4FBF-9B8E-911306264DE7Q57976164-354A514E-E1F4-46FE-B29C-460CCF91F465Q57976168-262C6A14-13E7-4DE7-B4AF-DAFF21755DF5Q57976171-822E7968-F7FC-4556-B604-39D670E60156Q57976178-E5178E7F-DF2F-4C7D-A9BC-B8D26CDA9C62Q57976179-4225AC8B-CC8A-4A3F-ACC6-B4AF6C224326Q57976190-398BE38F-58F2-4A32-941A-B2A1EE35FA5AQ57976198-C6CAA576-88AC-48B6-9B4D-1BE3AD70FE75Q57976203-D9EFCEC9-5E30-4B20-9862-E1FE41D45B42Q57976206-05C57C94-8AB9-4A23-8455-8ADF30F2CDD8Q57976208-16619E17-D8FF-41F6-8F3D-D487DDA45C1AQ57976244-6D47702D-C85E-415F-A4BF-EBF1745F888AQ57976248-E1CC7EEF-7090-4BFA-A4BF-E49672184684Q57976251-6C9E03A1-BF16-49FC-BE61-0D1B182EC226Q57976255-8E4D5D01-37AB-4640-9CED-CDFAFE5C82ADQ57976260-7D6C84C9-19C2-49D1-B47E-2729F94D2219Q89061515-1ECA1E1D-60BF-4CF4-9F99-7F96F6C4FC6FQ90866732-3E8F241E-BAAF-469B-AD3D-9036F3DBD79CQ92771309-07F842DB-51CD-454D-9B00-F914314CF77D
P50
description
Forscher
@de
chercheur
@fr
investigador
@es
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
研究者
@zh
name
Pedro M. P. Gois
@ast
Pedro M. P. Gois
@en
Pedro M. P. Gois
@es
Pedro M. P. Gois
@nl
type
label
Pedro M. P. Gois
@ast
Pedro M. P. Gois
@en
Pedro M. P. Gois
@es
Pedro M. P. Gois
@nl
prefLabel
Pedro M. P. Gois
@ast
Pedro M. P. Gois
@en
Pedro M. P. Gois
@es
Pedro M. P. Gois
@nl
P1053
A-9251-2014
P106
P1153
6507726637
P31
P3829
P496
0000-0002-7698-630X