IELO, Laura
 Distribuzione geografica
Continente #
NA - Nord America 241
EU - Europa 192
AS - Asia 112
AF - Africa 2
Totale 547
Nazione #
US - Stati Uniti d'America 241
IE - Irlanda 86
IT - Italia 49
CN - Cina 48
SG - Singapore 41
FR - Francia 18
SE - Svezia 15
SA - Arabia Saudita 7
DE - Germania 6
KR - Corea 6
UA - Ucraina 6
VN - Vietnam 4
IN - India 3
NL - Olanda 3
DK - Danimarca 2
GB - Regno Unito 2
GR - Grecia 2
HK - Hong Kong 2
NG - Nigeria 2
RS - Serbia 2
FI - Finlandia 1
JP - Giappone 1
Totale 547
Città #
Dublin 86
Medford 32
Princeton 26
Singapore 23
Hebei 19
Turin 14
Hangzhou 13
Wilmington 12
Torino 11
Beijing 8
Boston 8
Leawood 6
Seoul 6
Fairfield 5
Chandler 4
Falls Church 4
Como 3
Sondrio 3
Abuja 2
Aleksinac 2
Boardman 2
Catania 2
Chengdu 2
Easton 2
Hong Kong 2
New York 2
Norwalk 2
Perugia 2
Rome 2
Santa Clara 2
Wuhan 2
Ann Arbor 1
Ashburn 1
Baldissero Torinese 1
Cambridge 1
Carrù 1
Centro 1
Desio 1
Dong Ket 1
Guiyang 1
Jacksonville 1
Kangra 1
Lappeenranta 1
Lishui 1
London 1
Messina 1
Notre Dame 1
Piraeus 1
Pollena Trocchia 1
Redmond 1
San Diego 1
San Mauro Torinese 1
Seattle 1
Stockholm 1
Upper Marlboro 1
Villeneuve-d'Ascq 1
Totale 334
Nome #
Consecutive C1-Homologation / Displacement Strategy for Converting Thiosulfonates into O,S-Oxothioacetals 39
Chemoselective Homologation-Deoxygenation Strategy Enabling the Direct Conversion of Carbonyls into (n+1)-Halomethyl-Alkanes 38
Carbenoid-Mediated Homologation Tactics for Assembling (Fluorinated) Epoxides and Aziridines 36
Halogen-Imparted Reactivity in Lithium Carbenoid Mediated Homologations of Imine Surrogates: Direct Assembly of bis-Trifluoromethyl-β-Diketiminates and the Dual Role of LiCH2I 35
A Combination of Pharmacophore and Docking-based Virtual Screening to Discover new Tyrosinase Inhibitors 30
Electrophilicity Scale of Activated Amides: 17O NMR and 15N NMR Chemical Shifts of Acyclic Twisted Amides in N−C(O) Cross-Coupling 28
17O NMR and 15N NMR chemical shifts of sterically-hindered amides: Ground-state destabilization in amide electrophilicity 25
CHAPTER 9. Biomass-derived Solvents 24
Telescoped, Divergent, Chemoselective C1 and C1-C1 Homologation of Imine Surrogates: Access to Quaternary Chloro- and Halomethyl-Trifluoromethyl Aziridines 23
Straightforward chemoselective access to unsymmetrical dithioacetals through a thiosulfonate homologation-nucleophilic substitution sequence 22
Homologation chemistry with nucleophilic α-substituted organometallic reagents: Chemocontrol, new concepts and (solved) challenges 22
Merging lithium carbenoid homologation and enzymatic reduction: A combinative approach to the HIV-protease inhibitor Nelfinavir 21
Expeditious and Chemoselective Synthesis of α-Aryl and α-Alkyl Selenomethylketones via Homologation Chemistry 20
Taking advantage of lithium monohalocarbenoid intrinsic α-elimination in 2-MeTHF: controlled epoxide ring-opening en route to halohydrins 19
4-Fluorobenzylpiperazine-Containing Derivatives as Efficient Inhibitors of Mushroom Tyrosinase 19
Substituted α-Sulfur Methyl Carbanions: Effective Homologating Agents for the Chemoselective Preparation of β-Oxo Thioethers from Weinreb Amides 19
Exploiting the 1-(4-fluorobenzyl)piperazine fragment for the development of novel tyrosinase inhibitors as anti-melanogenic agents: Design, synthesis, structural insights and biological profile 18
Chemical exploration of 4-(4-fluorobenzyl)piperidine fragment for the development of new tyrosinase inhibitors 18
Evaluation of 4-(4-Fluorobenzyl)piperazin-1-yl]-Based Compounds as Competitive Tyrosinase Inhibitors Endowed with Antimelanogenic Effects 18
Direct and straightforward transfer of C1 functionalized synthons to phosphorous electrophiles for accessinggem-P-containing methanes 17
Direct Access to 9-Chloro-1 H-benzo[ b]furo[3,4- e]azepin-1-ones via Palladium(II)-Catalyzed Intramolecular syn-Oxypalladation/Olefin Insertion/sp2-C-H Bond Activation Cascade 16
The synthetic versatility of the Tiffeneau–Demjanov chemistry in homologation tactics 16
α-Arylamino Diazoketones: Diazomethane-Loading Controlled Synthesis, Spectroscopic Investigations, and Structural X-ray Analysis 16
Weinreb Amides as Privileged Acylating Agents for Accessing α-Substituted Ketones 13
Inhibition of HIV-1 RT activity by a new series of 3-(1,3,4-thiadiazol-2-yl)thiazolidin-4-one derivatives 13
Targeting Tyrosinase: Development and Structural Insights of Novel Inhibitors Bearing Arylpiperidine and Arylpiperazine Fragments 12
Selective noncovalent proteasome inhibiting activity of trifluoromethyl-containing gem-quaternary aziridines 8
Novel Class of Proteasome Inhibitors: In Silico and In Vitro Evaluation of Diverse Chloro(trifluoromethyl)aziridines 7
Biocatalysis in Green Biosolvents 6
Heterocyclic Compounds as Synthetic Tyrosinase Inhibitors: Recent Advances 5
Leveraging the 3-Chloro-4-fluorophenyl Motif to Identify Inhibitors of Tyrosinase from Agaricus bisporus 4
Syntheses, reactivity, and biological applications of coumarins 3
Recent advances in the accessibility, synthetic utility, and biological applications of aziridines 3
Lithium Carbenoids in Homologation Chemistry 3
Synthesis, computational investigation and biological evaluation of α,α-difluoromethyl ketones embodying pyrazole and isoxazole nuclei as COX inhibitors 2
Totale 618
Categoria #
all - tutte 4.174
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 4.174


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202140 0 0 0 0 0 0 13 5 7 0 5 10
2021/2022269 0 0 7 7 14 0 63 57 24 4 33 60
2022/2023147 28 2 6 0 4 56 25 2 10 2 5 7
2023/2024160 22 36 15 7 9 6 5 0 0 18 3 39
2024/20252 2 0 0 0 0 0 0 0 0 0 0 0
Totale 618