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Catalogo UNIPR: [129889] Home page macrotipologia

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1 Articolo su rivista 74736
- 1.1 Articolo su rivista 71066
- 1.2 Recensione 1389
- 1.3 Scheda bibliografica 72
- 1.4 Nota a sentenza 371
- 1.5 Abstract in Rivista 1785
- 1.6 Traduzione Rivista 53

2 Contributo in volume (Capitolo di libro) 17883
- 2.1 Contributo in volume (Capitolo di libro) 16430
- 2.2 Prefazione/Postfazione 378
- 2.3 Breve introduzione 146
- 2.4 Voce di enciclopedia 720
- 2.5 Traduzione in Volume 93
- 2.6 Schede di catalogo, repertorio o corpus 116

3 Libro (Monografia) 3618
- 3.1 Monografia, trattato scientifico 3322
- 3.2 Concordanza 0
- 3.3 Indice 11
- 3.4 Bibliografia 15
- 3.5 Edizione critica 105
- 3.6 Pubblicazione di fonti inedite 13
- 3.7 Commento scientifico 20
- 3.8 Traduzione di Libro 132

4 Contributo in atti di convegno (Proceedings) 28568
- 4.1a Atto convegno Rivista 2592
- 4.1b Atto convegno Volume 21806
- 4.2 Abstract in Atti di Convegno 3361
- 4.3 Poster 752
- 4.4 Intervento a convegno non pubblicato 57

5 Brevetto 475
- 5.1 Brevetto concesso 343
- 5.2 Domanda di brevetto 132

6 Curatela 1934
- 6.1 Cura di collana 168
- 6.2 Cura di libro 1329
- 6.3 Cura di numero di Rivista 240
- 6.4a Cura di atti di convegno Rivista 25
- 6.4b Cura di atti di convegno Volume 172

7 Altro 2675
- 7.01 Composizione 3
- 7.02 Disegno 2
- 7.03 Design 1
- 7.04 Performance 8
- 7.05 Esposizione 17
- 7.06 Mostra (Catalogo) 48
- 7.07 Manufatto 0
- 7.08 Prototipo d'arte,relativi progetti 2
- 7.09 Carta, Mappa 37
- 7.10 Banca dati 23
- 7.11 Software 31
- 7.12 Altro 2264
- 7.13 Prodotto multimediale 83
- 7.14 Progetto,piano,prodotto design 55
- 7.15 Rilievo architettonico 41
- Traduzione 61

8 Tesi di dottorato 0
- 8.1 Tesi di dottorato 0

Prodotti recenti

Aliphatic Aldehydes as CO Surrogates via Photocatalyzed Hydrogen Atom Transfer

The introduction of a carbonyl group enables smooth access to a wide plethora of bulk chemicals such as ketones, amides and esters[1]. The use of carbon monoxide (CO) is ideal for large-scale carbonylation in industry, where infrastructure allows its safe and efficient handling[2]. However, most academic laboratories lack the expertise and equipment required to safely manage even small amounts of this lethal gas, thus inhibiting methodological development. A controlled release of carbon mono...

A unified approach for the synthesis of 5-membered heteroaromatics by combining decatungstate photocatalysis and Paal-Knorr reaction in flow

Heteroaromatic compounds are highly sought after in pharmaceuticals, agrochemicals, and materials science, making the rapid synthesis of these molecules crucial. A key approach to accessing these valuable motifs is the Paal-Knorr method, particularly for synthesizing five-membered heterocyclic compounds such as furans, thiophenes, pyrroles. This method relies on the availability of 1,4-diketones. As a result, considerable efforts have been made to develop efficient strategies for preparing su...

Artificial metalloenzymes based on the Spy system exhibit versatile catalytic functions, from catecholase activity to hydrogen evolution

Metalloproteins catalyze some of the most complex biochemical transformations in nature. This study explores the rational redesign of the Spy system, comprising a peptide (SpyTag) that spontaneously forms a covalent isopeptide bond with its protein partner (SpyCatcher), yielding a stable recombinant Spy protein. The modular architecture of the system offers distinct advantages for the development of artificial metalloenzymes: the peptide segment permits the strategic incorporation of met...

Engineering the SpyTag peptide for artificial stereoselective metalloenzymes: copper coordination and catalytic function

"Metalloproteins facilitate some of the most intricate biological processes in nature. The project described here involves the redesign of the Spy complex, which comprises a peptide (SpyTag) that forms an isopeptide bond with a protein (SpyCatcher), resulting in a recombined Spy protein (Figure 1a). The peptide component allows for the straightforward incorporation of metal-binding sites into the final protein without the need to redesign the entire structure. Additionally, peptides can be sy...

SpyTag peptides: focus on copper binding and stereoselective oxidase activity

Metalloproteins promote some of the most complex biomolecular processes in nature. We present here results related to the redesign of the Spy protein into an artificial metalloenzyme. The Spy protein consists of a peptide (SpyTag) that spontaneously binds to a protein (SpyCatcher) through an isopeptide bond, to give rise to a recombined Spy protein (figura1a). The reason of the choice of this construct for devising a new artificial metalloenzyme is two-fold. On one hand the peptide compo...

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Catalogo UNIPR: [129889] Home page macrotipologia

Prodotti recenti

Aliphatic Aldehydes as CO Surrogates via Photocatalyzed Hydrogen Atom Transfer

A unified approach for the synthesis of 5-membered heteroaromatics by combining decatungstate photocatalysis and Paal-Knorr reaction in flow

Artificial metalloenzymes based on the Spy system exhibit versatile catalytic functions, from catecholase activity to hydrogen evolution

Engineering the SpyTag peptide for artificial stereoselective metalloenzymes: copper coordination and catalytic function

SpyTag peptides: focus on copper binding and stereoselective oxidase activity

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