RE.PUBLIC@POLIMI pubblicazioni di ricerca del Politecnico di Milano

GATTI, FRANCESCO GILBERTO
 Distribuzione geografica
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Continente #
NA - Nord America 848
EU - Europa 384
AS - Asia 151
SA - Sud America 17
AF - Africa 14
OC - Oceania 5
Totale 1419
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Nazione #
US - Stati Uniti d'America 819
IT - Italia 208
CN - Cina 40
IN - India 39
GB - Regno Unito 31
VN - Vietnam 28
DE - Germania 24
FR - Francia 24
NL - Olanda 20
ES - Italia 18
CA - Canada 17
IR - Iran 13
ZA - Sudafrica 12
JP - Giappone 9
CL - Cile 7
HN - Honduras 7
DK - Danimarca 6
PT - Portogallo 6
RO - Romania 6
SE - Svezia 6
TW - Taiwan 6
AR - Argentina 5
AT - Austria 5
AU - Australia 5
IE - Irlanda 5
MX - Messico 5
MY - Malesia 5
HK - Hong Kong 4
KR - Corea 4
PL - Polonia 4
CO - Colombia 3
CZ - Repubblica Ceca 3
FI - Finlandia 3
GR - Grecia 3
SK - Slovacchia (Repubblica Slovacca) 3
UA - Ucraina 3
BR - Brasile 2
ID - Indonesia 2
BE - Belgio 1
CH - Svizzera 1
HU - Ungheria 1
IL - Israele 1
LT - Lituania 1
LV - Lettonia 1
RU - Federazione Russa 1
SC - Seychelles 1
TN - Tunisia 1
Totale 1419
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Città #
Fairfield 85
Houston 84
Santa Cruz 62
Milan 60
Ann Arbor 49
Buffalo 42
Ashburn 37
Woodbridge 36
Seattle 33
Wilmington 33
Cambridge 29
Dong Ket 21
Beijing 15
Los Angeles 11
Las Vegas 10
Bengaluru 9
Chicago 9
Council Bluffs 9
Muizenberg 9
Barcelona 8
Mountain View 8
Atlanta 7
Boardman 7
Centro 7
Clearwater 7
Fleming Island 7
Groningen 7
Ottawa 7
Brescia 6
Phoenix 6
Dallas 5
Delft 5
Lisbon 5
London 5
New York 5
San Francisco 5
Sesto San Giovanni 5
Shanghai 5
Toronto 5
Wuhan 5
Bari 4
Basking Ridge 4
Chennai 4
Detroit 4
Dublin 4
Henderson 4
Lake Forest 4
Nanjing 4
Nottingham 4
Paris 4
Pordenone 4
Rome 4
San Diego 4
Stanford 4
Arese 3
Bogotá 3
Copenhagen 3
Corvallis 3
Crugers 3
Duncan 3
Fars 3
Hangzhou 3
Helsinki 3
Lavagno 3
Lincoln 3
Liverpool 3
Milpitas 3
Mumbai 3
Padova 3
Reston 3
Tokyo 3
Turin 3
University Park 3
Vienna 3
Zavalla 3
Austin 2
Baranzate 2
Belfast 2
Bergamo 2
Besano 2
Bologna 2
Boston 2
Boulder 2
Brierley Hill 2
Burgos 2
Campi Bisenzio 2
Delhi 2
Genova 2
Gurgaon 2
Hyderabad 2
Jakarta 2
La Jolla 2
Lyon 2
Madison 2
Manchester 2
Monmouth Junction 2
Mount Olive 2
Münster 2
Niagara Falls 2
Oviedo 2
Totale 939
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Nome #
Exploiting the vicinal disubstituent effect on the diastereoselective synthesis of γ and δ lactones, file e0c31c0d-2dd1-4599-e053-1705fe0aef77 224
Chemo-Enzymatic Oxidative Rearrangement of Tertiary Allylic Alcohols: Synthetic Application and Integration into a Cascade Process, file e0c31c10-cffe-4599-e053-1705fe0aef77 157
Biocatalytic synthesis of chiral cyclic gamma-oxoesters by sequential C-H hydroxylation, alcohol oxidation and alkene reduction, file e0c31c0b-b376-4599-e053-1705fe0aef77 124
One-pot multi-enzymatic synthesis of the four stereoisomers of 4-methylheptan-3-ol, file e0c31c0b-725d-4599-e053-1705fe0aef77 119
Biocatalytic approach to chiral beta-nitroalcohols by enantioselective alcohol dehydrogenase-mediated reduction of alpha-nitroketones, file e0c31c0d-80ab-4599-e053-1705fe0aef77 114
Stereoselective synthesis of hernandulcin, peroxylippidulcine A, lippidulcines A, B and C and taste evaluation, file e0c31c08-c532-4599-e053-1705fe0aef77 111
Conversion of oleic acid into azelaic and pelargonic acid by a chemo-enzymatic route, file e0c31c0f-9641-4599-e053-1705fe0aef77 103
Chemoselective Biohydrogenation of Alkenes in the Presence of Alkynes for the Homologation of 2-Alkynals/3-Alkyn-2-ones into 4-Alkynals/Alkynols, file e0c31c0f-3630-4599-e053-1705fe0aef77 101
Reactive Deep Eutectic Solvents (RDESs): A New Tool for Phospholipase D-Catalyzed Preparation of Phospholipids, file e0c31c11-333b-4599-e053-1705fe0aef77 84
Stereoselectivity switch in the reduction of α-Alkyl-β-arylenones by structure-guided designed variants of the ene reductase OYE1, file e0c31c0f-3633-4599-e053-1705fe0aef77 67
Enantioselective Synthesis of (R)-2-Arylpropanenitriles Catalysed by Ene-Reductases in Aqueous Media and in Biphasic Ionic Liquid–Water Systems, file e0c31c0d-a864-4599-e053-1705fe0aef77 57
Opposite Enantioselectivity in the Bioreduction of (Z)-beta-Aryl-eta-cyanoacrylates Mediated by the Tryptophan 116 Mutants of Old Yellow Enzyme 1: Synthetic Approach to (R)- and (S)-beta-Aryl-gamma-lactams, file e0c31c10-95c1-4599-e053-1705fe0aef77 49
Multi-enzyme cascade synthesis of the most odorous stereoisomers of the commercial odorant Muguesia, file e0c31c0e-0722-4599-e053-1705fe0aef77 40
Chemoenzymatic Synthesis of Enantioenriched (R)‐ and (S)‐Aryloxyalkanoic Herbicides, file 04a1ef2b-3279-441f-a570-9eb0423f226c 26
Rationalisation of the stereochemical outcome of ene-reductase-mediated bioreduction of α,β-difunctionalised alkenes, file e0c31c0d-d26a-4599-e053-1705fe0aef77 26
Exploitation of a Multienzymatic Stereoselective Cascade Process in the Synthesis of 2-Methyl-3-Substituted Tetrahydrofuran Precursors, file e0c31c10-ae1d-4599-e053-1705fe0aef77 21
Cascade Coupling of Ene-Reductases and w-Transaminases for the Stereoselective Synthesis of Diastereomerically Enriched Amines, file e0c31c10-d000-4599-e053-1705fe0aef77 17
“A Study in Yellow”: Investigations in the Stereoselectivity of Ene-Reductases, file e0c31c12-6ec7-4599-e053-1705fe0aef77 15
Substrate-engineering approach to the stereoselective chemo-multienzymatic cascade synthesis of Nicotiana tabacum lactone, file e0c31c10-d2a4-4599-e053-1705fe0aef77 13
Synthesis of Polycyclic Fused Indoline Scaffolds through a Substrate-Guided Reactivity Switch, file e0c31c12-d232-4599-e053-1705fe0aef77 9
Multi-enzyme cascade synthesis of the most odorous stereoisomers of the commercial odorant Muguesia, file e0c31c08-bb87-4599-e053-1705fe0aef77 4
Multienzymatic Stereoselective Reduction of Tetrasubstituted Cyclic Enones to Halohydrins with Three Contiguous Stereogenic Centers, file 380f6999-20de-469f-b592-de3d12d0cb2c 3
Rationalisation of the stereochemical outcome of ene-reductase-mediated bioreduction of α,β-difunctionalised alkenes, file e0c31c08-2023-4599-e053-1705fe0aef77 3
Synthesis of Robalzotan, Ebalzotan, and Rotigotine Precursors via the Stereoselective Multienzymatic Cascade Reduction of α,β-Unsaturated Aldehydes, file e0c31c08-120d-4599-e053-1705fe0aef77 2
Enantioselective Synthesis of (R)-2-Arylpropanenitriles Catalysed by Ene-Reductases in Aqueous Media and in Biphasic Ionic Liquid–Water Systems, file e0c31c08-2809-4599-e053-1705fe0aef77 2
Opposite Enantioselectivity in the Bioreduction of (Z)-beta-Aryl-eta-cyanoacrylates Mediated by the Tryptophan 116 Mutants of Old Yellow Enzyme 1: Synthetic Approach to (R)- and (S)-beta-Aryl-gamma-lactams, file e0c31c0f-ce67-4599-e053-1705fe0aef77 2
Cascade Coupling of Ene-Reductases and w-Transaminases for the Stereoselective Synthesis of Diastereomerically Enriched Amines, file e0c31c10-d2ab-4599-e053-1705fe0aef77 2
Enoate Reductase-Mediated Preparation of Methyl (S)-2-Bromobutanoate, a Useful Key Intermediate for the Synthesis of Chiral Active Pharmaceutical Ingredients, file e0c31c07-f0e2-4599-e053-1705fe0aef77 1
Steric Effects on the Stereochemistry of Old Yellow Enzyme-Mediated Reductions of Unsaturated Diesters: Flipping of the Substrate within the Enzyme Active Site Induced by Structural Modifications, file e0c31c07-fbd4-4599-e053-1705fe0aef77 1
Exploitation of a Multienzymatic Stereoselective Cascade Process in the Synthesis of 2-Methyl-3-Substituted Tetrahydrofuran Precursors, file e0c31c10-89eb-4599-e053-1705fe0aef77 1
Exploitation of Soybean Oil Acid Degumming Waste: Biocatalytic Synthesis of High Value Phospholipids, file e0c31c11-6576-4599-e053-1705fe0aef77 1
Chemo-enzymatic oxidative cleavage of isosafrole for the synthesis of piperonal, file e0c31c12-5c81-4599-e053-1705fe0aef77 1
Dependence of 1H-NMR T1 relaxation time of trimethylglycine betaine deep eutectic solvents on the molar composition and on the presence of water, file efe30bf9-9317-402d-a26b-0556f28c2d4f 1
Totale 1501
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Categoria #
all - tutte 2408
article - articoli 2408
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 4816
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/20183 0000 00 00 3000
2018/201978 0030 00 01 473033
2019/2020231 2691011 178 2925 31152723
2020/2021305 26161921 1613 1926 40462340
2021/2022466 27146563 5415 2227 33308531
2022/2023412 33439852 3931 6334 19000
Totale 1501