| Nome |
# |
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Outstanding Chiroptical Features of Thin Films of Chiral Oligothiophenes, file e0d6c92c-340d-fcf8-e053-d805fe0aa794
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279
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Cyclization Reactions for the Synthesis of Phthalans and Isoindolines, file e0d6c92d-c1b4-fcf8-e053-d805fe0aa794
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213
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|
null, file e0d6c92e-83d3-fcf8-e053-d805fe0aa794
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212
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|
Synthesis of Functionalised 3-Isochromanones by Silylcarbocyclisation/Desilylation Reactions, file e0d6c92c-30e1-fcf8-e053-d805fe0aa794
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186
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null, file e0d6c92c-28d6-fcf8-e053-d805fe0aa794
|
166
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|
null, file e0d6c92b-f8ce-fcf8-e053-d805fe0aa794
|
163
|
|
null, file e0d6c92c-0c3c-fcf8-e053-d805fe0aa794
|
156
|
|
Cyclocarbonylative Sonogashira Reactions of 1-Ethynylbenzyl Alcohols: Synthesis of 1-Carbonylmethylene-1,3-Dihydroisobenzofurans, file e0d6c92c-2856-fcf8-e053-d805fe0aa794
|
154
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Synthesis of 2-Alkylideneisochromans by Cyclocarbonylative Sonogashira Reactions, file e0d6c92b-f8d5-fcf8-e053-d805fe0aa794
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140
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null, file e0d6c92e-e014-fcf8-e053-d805fe0aa794
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133
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Acyl sonogashira cross-coupling: State of the art and application to the synthesis of heterocyclic compounds, file e0d6c92e-93d5-fcf8-e053-d805fe0aa794
|
118
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Supramolecular organization of new chiral π-conjugated oligomers: synthesis and spectroscopic study, file e0d6c927-d272-fcf8-e053-d805fe0aa794
|
89
|
|
null, file e0d6c92c-30df-fcf8-e053-d805fe0aa794
|
88
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Potentiality and Synthesis of O- and N-Heterocycles: Pd-Catalyzed Cyclocarbonylative Sonogashira Coupling as aValuable Route to Phthalans, Isochromans, and Isoindolines, file e0d6c92e-d23e-fcf8-e053-d805fe0aa794
|
37
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Chiroptical response inversion upon sample flipping in thin films of a chiral benzo[1,2-b:4,5-b′]dithiophene-based oligothiophene, file 17f2fba9-d863-4640-a513-3c54bde8cb78
|
16
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Synthesis of new bis[1-(thiophenyl)propynones] as potential organic dyes for colorless luminescent solar concentrators (LSCs), file 4fbcc491-76a1-43aa-8b87-4ddf66f59a1f
|
10
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Synthesis of N-Heteroaromatic Compounds through Cyclocarbonylative Sonogashira Reactions, file 90847f60-bd28-4f06-bd64-cff13a3dcfa2
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9
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Chiral oligothiophenes for optoelectronic applications: synthesis and spectroscopic study of supramolecular aggregation, file e0d6c927-e3c1-fcf8-e053-d805fe0aa794
|
8
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Photophysical properties of new p-phenylene- and benzodithiophene-based fluorophores for luminescent solar concentrators (LSCs), file a87d1110-25cd-4fb9-beae-a89c88d1f5b1
|
7
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Palladium nanoparticles supported on smopex-234® as valuable catalysts for the synthesis of heterocycles, file a699fe34-9d99-4d9f-9cb4-643b877bf8f9
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6
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Metal Promoted Cyclocarbonylation Reactions in the Synthesis of Heterocycles, file e0d6c931-b014-fcf8-e053-d805fe0aa794
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6
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Tris-Ethynylphenyl-amine Fluorophores: Synthesis,
Characterisation and Test of Performances in Luminescent
Solar Concentrators, file e0d6c92c-32ff-fcf8-e053-d805fe0aa794
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5
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null, file e0d6c928-8969-fcf8-e053-d805fe0aa794
|
4
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Synthesis and characterization of new chiral oligothiophenes for innovative optoelectronic applications, file e6a6f544-44ca-4943-b634-5f2530e11da4
|
4
|
|
Palladium nanoparticles supported on Smopex®metal scavengers ascatalyst for carbonylative Sonogashira reactions: Synthesis of α,β-alkynyl ketones, file 690d1ef4-f364-47cb-8525-a22dc41465da
|
2
|
|
null, file 9f7051b0-c1b1-446c-adbd-a0fe422e584c
|
2
|
|
null, file c85d85ab-5a04-414f-8507-764cc114fc2c
|
2
|
|
null, file e0d6c92f-4980-fcf8-e053-d805fe0aa794
|
2
|
|
null, file e0d6c92f-54f5-fcf8-e053-d805fe0aa794
|
2
|
|
Chiral Oligothiophenes with Remarkable Circularly Polarized Luminescence and Electroluminescence in Thin Films, file e0d6c92f-dbb2-fcf8-e053-d805fe0aa794
|
2
|
|
Transition Metal Promoted Synthesis of Isoindoline Derivatives, file 404102b5-f441-4cc8-8f86-f5f2025a2983
|
1
|
|
null, file 99198a9d-5d6c-4812-a226-74d1ed6c73d7
|
1
|
|
null, file b2ff9e69-a53e-419e-9bc7-7738b9367803
|
1
|
|
Outstanding chiroptical features in thin films of new chiral π-conjugated oligomers, file e0d6c92b-20d9-fcf8-e053-d805fe0aa794
|
1
|
|
Synthesis of novel chiral oligothiophenes showing outstanding chiroptical properties in thin films, file e0d6c92b-20e1-fcf8-e053-d805fe0aa794
|
1
|
|
null, file e0d6c92b-f529-fcf8-e053-d805fe0aa794
|
1
|
|
null, file e0d6c92c-0763-fcf8-e053-d805fe0aa794
|
1
|
|
Synthesis of Functionalised Indoline and Isoquinoline Derivatives through a Silylcarbocyclisation/Desilylation Sequence, file e0d6c92c-1001-fcf8-e053-d805fe0aa794
|
1
|
|
null, file e0d6c92c-271c-fcf8-e053-d805fe0aa794
|
1
|
|
null, file e0d6c931-36ae-fcf8-e053-d805fe0aa794
|
1
|
|
Supported Metal Catalysts for the Synthesis of N-Heterocycles, file e0d6c932-1a25-fcf8-e053-d805fe0aa794
|
1
|
|
null, file eea5ab2c-ad8a-4aed-be82-0ed302488f25
|
1
|
|
null, file f1d15101-129d-4f45-9e38-4a60a0204d28
|
1
|
| Totale |
2234 |