about
Green chemistry with selenium reagents: development of efficient catalytic reactionsArylation with unsymmetrical diaryliodonium salts: a chemoselectivity studyClick-chemistry approaches to π-conjugated polymers for organic electronics applications.Catalytic Asymmetric Reactions of 4-Substituted Indoles with Nitroethene: A Direct Entry to Ergot Alkaloid Structures.A Catalytic Peterson-like Synthesis of Alkenyl Nitriles.PS-BEMP as a basic catalyst for the phospha-Michael addition to electron-poor alkenes.Elucidation of Mechanisms and Selectivities of Metal-Catalyzed Reactions using Quantum Chemical Methodology.Heterogeneous C–H alkenylations in continuous-flow: oxidative palladium-catalysis in a biomass-derived reaction mediumWaste Minimized Multistep Preparation in Flow of β-Amino Acids Starting from α,β-Unsaturated Carboxylic AcidsEnantioselective organocatalytic substitution of alpha-cyanoacetates on imidoyl chlorides--synthesis of optically active ketiminesCationic cyclization of 2-alkenyl-1,3-dithiolanes: diastereoselective synthesis of trans-decalinsSynthetic studies on the solanacol ABC ring system by cation-initiated cascade cyclization: implications for strigolactone biosynthesisA general phosphoric acid-catalyzed desymmetrization of meso-aziridines with silylated selenium nucleophilesTheoretical study of mechanism and selectivity of copper-catalyzed C-H bond amidation of indolesEnzyme-like catalysis via ternary complex mechanism: alkoxy-bridged dinuclear cobalt complex mediates chemoselective O-esterification over N-amidationTheoretical study of mechanism and stereoselectivity of catalytic Kinugasa reactionTowards Sustainable C-H Functionalization Reactions: The Emerging Role of Bio-Based Reaction MediaC-H functionalization reactions under flow conditions
P50
Q28260426-162F5E6F-FEC4-47B2-A4E7-614FF521ADEDQ37449351-F17AD932-5E2E-43D8-A82F-F6BAE4194F25Q39342746-CA2EDD99-2197-4475-A314-D5D59BD0EFBFQ40214288-EB1DA86F-9625-426E-943D-497032504E87Q50427045-EBB0127B-9894-4D3B-8D09-08447A4AC1FAQ50428300-7984BC59-6F6E-47B4-892E-06E936A20DA5Q53139361-95834E10-7B01-41F6-B502-C0F6606D418AQ58656174-A584E3F5-BE13-4E2E-97A6-98009F340F94Q60491646-CCCC359A-0162-4B77-943A-812F2D74024FQ80148235-CC1EE0FB-F524-4D37-A0F3-33C12A985EE9Q83741336-82FF5961-F8B0-40FB-ACC4-89FA673F01ADQ84448727-5DBFD365-C40F-4085-A341-2A2D340CF49AQ84606019-1B3F2B5C-9E0E-4BB4-86B4-B719B96393FDQ85053027-053C53E9-088F-4006-A999-2345CB7AA171Q86586619-02ECBDA4-3F8A-4C0D-AC38-BFDBC0D83931Q86668206-BADCFAC0-3495-4BBC-9116-01108BDD7CAEQ88395181-33A42C65-5A26-487D-83CB-750618639EAEQ92817745-BB38F4CA-CE0F-4F0D-9882-E13C75FF6F40
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Stefano Santoro
@ast
Stefano Santoro
@en
Stefano Santoro
@es
Stefano Santoro
@nl
Stefano Santoro
@sl
type
label
Stefano Santoro
@ast
Stefano Santoro
@en
Stefano Santoro
@es
Stefano Santoro
@nl
Stefano Santoro
@sl
prefLabel
Stefano Santoro
@ast
Stefano Santoro
@en
Stefano Santoro
@es
Stefano Santoro
@nl
Stefano Santoro
@sl
P1053
C-5001-2009
P106
P1153
22942136300
P21
P31
P496
0000-0003-0223-1489