COLELLA, MARCO
 Distribuzione geografica
Continente #
NA - Nord America 2.365
AS - Asia 1.611
EU - Europa 1.202
SA - Sud America 357
Continente sconosciuto - Info sul continente non disponibili 317
AF - Africa 89
OC - Oceania 3
Totale 5.944
Nazione #
US - Stati Uniti d'America 2.254
SG - Singapore 598
IT - Italia 414
BR - Brasile 289
CN - Cina 288
HK - Hong Kong 236
RU - Federazione Russa 161
VN - Vietnam 134
DE - Germania 119
GB - Regno Unito 115
FR - Francia 103
SE - Svezia 84
CA - Canada 75
IN - India 60
JP - Giappone 54
TW - Taiwan 46
CI - Costa d'Avorio 32
ID - Indonesia 30
FI - Finlandia 29
BD - Bangladesh 28
NL - Olanda 28
KR - Corea 25
BE - Belgio 24
AR - Argentina 23
AT - Austria 23
PK - Pakistan 21
ZA - Sudafrica 20
ES - Italia 19
MX - Messico 19
IQ - Iraq 14
PL - Polonia 14
CO - Colombia 11
TR - Turchia 11
EC - Ecuador 10
SA - Arabia Saudita 9
UZ - Uzbekistan 9
CL - Cile 8
HU - Ungheria 7
IE - Irlanda 7
LT - Lituania 7
MA - Marocco 7
PH - Filippine 7
VE - Venezuela 7
NP - Nepal 6
RO - Romania 6
TN - Tunisia 6
UA - Ucraina 6
AE - Emirati Arabi Uniti 5
CH - Svizzera 5
EE - Estonia 5
KE - Kenya 5
SY - Repubblica araba siriana 5
DK - Danimarca 4
DZ - Algeria 4
PT - Portogallo 4
AL - Albania 3
AU - Australia 3
CZ - Repubblica Ceca 3
ET - Etiopia 3
GA - Gabon 3
GE - Georgia 3
GT - Guatemala 3
IL - Israele 3
JM - Giamaica 3
MY - Malesia 3
PY - Paraguay 3
SK - Slovacchia (Repubblica Slovacca) 3
AO - Angola 2
BG - Bulgaria 2
BO - Bolivia 2
CR - Costa Rica 2
CY - Cipro 2
DO - Repubblica Dominicana 2
EG - Egitto 2
IR - Iran 2
LV - Lettonia 2
LY - Libia 2
NO - Norvegia 2
PE - Perù 2
QA - Qatar 2
SV - El Salvador 2
TH - Thailandia 2
AI - Anguilla 1
AM - Armenia 1
BH - Bahrain 1
BW - Botswana 1
BY - Bielorussia 1
CW - ???statistics.table.value.countryCode.CW??? 1
GP - Guadalupe 1
GR - Grecia 1
GY - Guiana 1
HN - Honduras 1
JO - Giordania 1
KG - Kirghizistan 1
KH - Cambogia 1
LA - Repubblica Popolare Democratica del Laos 1
MD - Moldavia 1
MN - Mongolia 1
NI - Nicaragua 1
OM - Oman 1
Totale 5.624
Città #
Ashburn 347
Singapore 335
San Jose 226
Hong Kong 187
Chandler 125
New York 112
Fairfield 102
Beijing 92
Milan 82
Los Angeles 77
Santa Clara 76
Seattle 61
Nyköping 58
Houston 56
Bari 54
Woodbridge 50
Phoenix 46
Cambridge 44
Tokyo 42
Dallas 41
Ho Chi Minh City 36
Lauterbourg 36
Wilmington 36
Council Bluffs 33
Draper 33
Abidjan 32
Dong Ket 32
Nottingham 31
Frankfurt am Main 29
Rome 29
São Paulo 29
Columbus 26
Munich 26
London 25
Ningbo 25
Brooklyn 24
Buffalo 24
Falkenstein 23
Boardman 22
Chicago 22
Jakarta 22
Cedar Knolls 20
Helsinki 18
Brussels 17
Lawrence 17
Stockholm 17
Montreal 16
Ann Arbor 15
Fremont 15
Hanoi 15
Roxbury 15
Toronto 15
Denver 14
Moscow 14
Vienna 14
Amsterdam 13
Richardson 13
Warsaw 13
Figino 12
Shanghai 12
Chennai 11
Des Moines 11
Naples 11
Taichung 11
Taipei 11
Turin 11
Düsseldorf 10
Johannesburg 10
San Diego 10
The Dalles 10
Tukwila 10
Freiberg 9
Kaohsiung 9
Mexico City 9
Poplar 9
Pune 9
Québec 9
Vancouver 9
Belo Horizonte 8
Boston 8
Islamabad 8
Paris 8
Pescara 8
Rio de Janeiro 8
Wenzhou 8
Atlanta 7
Baghdad 7
Dublin 7
Haiphong 7
Orem 7
Ottawa 7
Portsmouth 7
Rouen 7
Tashkent 7
Turku 7
Victoria 7
Budapest 6
Da Nang 6
Evanston 6
Fragagnano 6
Totale 3.429
Nome #
1,3-Dibromo-1,1-difluoro-2-propanone as a Useful Synthon for a Chemoselective Preparation of 4-Bromodifluoromethyl Thiazoles 299
Development of a sustainable continuous flow synthesis of functionalized azetines and azetidines 228
Flow Chemistry as Enabling Technology for the Preparation of Functionalized 2-Azetines and Azetidines by Using a Common Synthetic Precursor 226
Synthesis and use of halodifluoromethyl heterocycles 221
1-Oxa-2,6-Diazaspiro[3.3]heptane as a New Potential Piperazine Bioisostere – Flow-Assisted Preparation and Derivatisation by Strain-Release of Azabicyclo[1.1.0]butanes 191
Use of flow technology for the development of a sustainable synthesis of azetines and azetidines 184
Exploiting a "Beast" in Carbenoid Chemistry: Development of a Straightforward Direct Nucleophilic Fluoromethylation Strategy 165
Modular and Chemoselective Strategy for the Direct Access to α-Fluoroepoxides and Aziridines via the Addition of Fluoroiodomethyllithium to Carbonyl-Like Compounds 155
Flow Microreactor Technology for Taming Highly Reactive Chloroiodomethyllithium Carbenoid: Direct and Chemoselective Synthesis of α-Chloroaldehydes 152
Use of Hypervalent Iodine in the Synthesis of Isomeric Dihydrooxazoles 149
Use of Flow Technologies and Photochemical Methods for the Preparation and Synthetic Manipulation of Functionalized Azetines 147
Hypervalent iodine (III) reagents and ammonia as useful combination for highly chemoselective N-transfer to low-valent organosulfur compounds and amines 145
Straightforward chemo- and stereoselective fluorocyclopropanation of allylic alcohols: Exploiting the electrophilic nature of the not so elusive fluoroiodomethyllithium 143
Continuous Flow Generation of Highly Reactive Organometallic Intermediates: A Recent Update 139
Stereo-and enantioselective addition of organolithiums to 2-oxazolinylazetidines as a synthetic route to 2-acylazetidines 137
Supported Catalysts for Continuous Flow Synthesis 136
Development of a Continuous Flow Synthesis of 2-Substituted Azetines and 3-Substituted Azetidines by Using a Common Synthetic Precursor 130
Synthesis of Biaryls Having a Piperidylmethyl Group Based on Space Integration of Lithiation, Borylation, and Suzuki–Miyaura Coupling 129
Sulfinimidate Esters as an Electrophilic Sulfinimidoyl Motif Source: Synthesis of N-Protected Sulfilimines from Grignard Reagents 125
A sustainable and chemoselective continuous flow hydrogenation of functionalized 2-azetines to azetidines 120
Synthesis of Sulfonimidamides from Sulfenamides via an Alkoxy-amino-λ6-sulfanenitrile Intermediate 120
Continuous flow synthesis of heterocycles: A recent update on the flow synthesis of indoles 119
(1R,2S,5R)-2-Isopropyl-5-methylcyclohexyl (R)-4-methylbenzenesulfonimidate 113
Structure-based design of multitargeting ChEs-MAO B inhibitors based on phenyl ring bioisosteres: AChE/BChE selectivity switch and drug-like characterization 107
A unified flow strategy for the preparation and use of trifluoromethyl-heteroatom anions 105
Flow Technology for the Genesis and Use of (Highly) Reactive Organometallic Reagents 105
Flow technology enabled preparation of C3-heterosubstituted 1-azabicyclo[1.1.0]butanes and azetidines: accessing unexplored chemical space in strained heterocyclic chemistry 103
Flow Microreactors and Photochemistry as Enabling Technologies for the Straightforward Preparation of Four-Membered Azaheterocycles 101
Preparation and Synthetic Manipulation of Four-Membered Aza-Heterocycles: New Strategies and Enabling Flow Technologies in Action 91
Unlocking geminal fluorohaloalkanes in nucleophilic fluoroalkylation chemistry: generation and trapping of lithiumfluorocarbenoids enabled by flow microreactors 88
Sustainable continuous flow synthesis of β-aminocarbonyls via acid-catalyzed hydration of N-Boc-2-azetines 87
Overlooked aza-S(iv) motifs: synthesis and transformations of sulfinamidines and sulfinimidate esters 85
N−N Bond Formation Using an Iodonitrene as an Umpolung of Ammonia: Straightforward and Chemoselective Synthesis of Hydrazinium Salts 84
Dynamic Phenomena and Complexation Effects in the α-Lithiation and Asymmetric Functionalization of Azetidines 83
FLOW MICROREATOR TECHONOLOGY AS UNIQUE TOOL FOR THE GENERATION AND USE OF (HIGHLY) REACTIVE ORGANOLITHIUM REAGENTS 80
The synthetic versatility of fluoroiodomethane: recent applications as monofluoromethylation platform 79
FLOW MICROREATORS AS ENABLING TECHNOLOGY FOR THE GENESIS AND USE OF (HIGHLY) REACTIVE ORGANOLITHIUM REAGENTS 78
Continuous Flow Generation of Highly Reactive Lithium-Fluorocarbenoids: A Straighforward Approach for Unprecedented Nucleophilic Fluoroalkylations 78
Forging C−S Bonds on the Azetidine Ring by Continuous Flow Photochemical Addition of Thiols and Disulfides to Azetines 76
Taming 3-Oxetanyllithium Using Continuous Flow Technology 76
Fluoro-Substituted Methyllithium Chemistry: External Quenching Method Using Flow Microreactors 75
Flow chemistry as enabling technology for controlling the reactivity of fluorocarbenoids 70
Synthesis of alcohols: streamlined C1 to Cn hydroxyalkylation through photoredox catalysis 69
Borylmetallation of alkynes made easy in flow 67
Microwave-Assisted Treatment of Waste Wood Biomass with Deep Eutectic Solvents 66
Lithiated three-membered heterocycles as chiral nucleophiles in the enantioselective synthesis of 1-oxaspiro[2,3]hexanes 60
Straightforward Tactics and Enabling Technologies as useful tools for Fluoroalkylations 57
Microreactor as enabling technology for taming highly reactive metal fluorocarbenoids 56
Straightforward Tactics and Enabling Technologies as useful tools for Fluoroalkylations 48
Straightforward Tactics and Enabling Technologies as Useful Tools for Fluoroalkylations 42
Lithium 31
Synthesis of Aza‐S(VI) Fluorides and Primary Sulfonimidamides from Sulfinylamines 23
Continuous Flow Decarboxylative Monofluoroalkylation Enabled by Photoredox Catalysis 20
Novel Sulfonium Reagents for the Modular Synthesis of Spiro[2.3]Hexanes and Heteroatom‐Containing Analogues: Synthesis, Application, and Evaluation as Bioisosteres 18
Tunable Preparation of α‐Aminoacyl Fluorides and α‐Fluoroamides via Base‐Induced Cascade Multiple‐Cleavage Processes from Bromodifluorohydrin Reagents and Amines 13
Azabicyclo[1.1.0]butyl‐Substituted Sulfonimidoyl Fluoride: Electrophilic Hub Bridging Late‐Stage Azetidine Incorporation with Sufex Chemistry 11
Leveraging multitargeting BChE-MAO B inhibitors against microglia-related neuroinflammation: in vitro biological evaluation, structure-activity relationships, drug-like properties, and X-ray crystal complexes 9
Generation and Use of Cyclopropenyllithium under Continuous Flow Conditions 7
Iodonitrene-Mediated Nitrogen Transfer to Alkenes for the Direct Synthesis of NH-Aziridines 7
Generation and Use of Bicyclo[1.1.0]butyllithium under Continuous Flow Conditions 6
Strained spiro heterocycles as potential bioisosteres: an update on the synthesis of heteroatom-containing spiro[2.3]hexanes and spiro[3.3]heptanes 5
Shifting Lithium Amide Reactivity to the Radical Domain: Regioselective Radical C−H Functionalization of 3‐Iodooxetane for the Synthesis of 1,5‐Dioxaspiro[2.3]hexanes 5
Totale 5.944
Categoria #
all - tutte 23.067
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 23.067


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022143 11 1 9 4 1 16 5 9 6 11 21 49
2022/2023361 37 37 16 29 35 31 3 35 39 5 90 4
2023/2024295 8 32 11 34 17 88 4 12 18 32 13 26
2024/20251.358 50 33 141 108 73 91 186 135 49 99 151 242
2025/20263.166 477 238 370 335 336 142 244 107 282 292 125 218
2026/202789 89 0 0 0 0 0 0 0 0 0 0 0
Totale 5.944