Curriculum Vitae

Professor Fabio Mantellini Università degli Studi di Urbino “Carlo Bo” Dipartimento di Scienze Biomolecolari,

Via I Maggetti 24, 61029 Urbino, Italy

Tel. 0722-303445 Studio; 0722-303446 Laboratorio

E-mail: fabio.mantellini@uniurb.it

Nato a Forli’ il 10 Maggio 1970

Il Prof. Fabio Mantellini ha conseguito la Laurea in Chimica Industriale presso la Facoltà di

Chimica Industriale dell'Università degli Studi di Bologna nell'anno accademico 1994-95,

discutendo la tesi sperimentale "Sintesi a temperatura ambiente di aza e 1,2-diaza eterocicli a varie

dimensioni usando una ciclocondensazione mediata da PCl3" con relatore il Chiar.mo Prof.

Graziano Baccolini..

Il Prof. Fabio Mantellini partecipa dal 1 Aprile 1996 alle attività di ricerca presso la Sezione di

Chimica Organica del ipartimento di Scienze Biomolecolari dell'Università di Urbino nel campo dei

derivati dell'idrazina e dei composti eterociclici contenenti l'atomo di azoto, zolfo, selenio.

Nell’ambito di queste ricerche, il Prof. Mantellini ha partecipato come collaboratore a diversi

progetti nazionali (PRIN 2003, PRIN 2004, PRIN 2005).

Il 6 Giugno 1996 ha conseguito l'abilitazione all'esercizio della professione di Chimico presso

l'Università degli Studi di Modena.

Nel 1999, nell‟ambito di un progetto di ricerca con il Prof Lutz F. Tietze il Prof. Fabio Mantellini si

è recato in Germania, presso la Georg-August-Universität di Göttingen in qualita di Visiting

Researcher, sviluppando una nuova procedura per la sintesi in fase solida di diversi nuclei

eterociclici. Ha inoltre collaborato in numerosi altri progetti di ricerca con gruppi stranieri facenti

riferimento a: Prof. Francisco Palacios (Spagna), Prof. Peter Langer (Germania), Prof. Vahuni

Karapetaìyan, (Armenia), Prof. Branko Stanovnik (Slovenia), Prof. Athina Geronikaki (Grecia),

Prof Carmen Najera (Spagna).

Dal 1 Novembre 2002 è ricercatore universitario (Settore scientifico-disciplinare: CHIM/06) presso

l'Istituto di Chimica Organica della Facoltà di Scienze Matematiche, Fisiche e Naturali

dell'Università di Urbino, essendo risultato vincitore di pubblico concorso per titoli ed esami.

Dal 1 Novembre 2013 è responsabile e coordinatore della Sezione di Chimica Organica e delle

Sostanze Organiche Naturali del Dipartimento di Scienze Biomolecolari dell'Università degli Studi

di Urbino “Carlo Bo”.

In data 11 Dicembre 2013 ha conseguito l’Abilitazione Nazionale Scientifica a Professore di II

Fascia nel settore scientifico disciplinare 03/C1 (Chimica Organica).

Dal 1 Novembre 2015 è professore associato (Settore scientifico-disciplinare: CHIM/06) presso il

Dipartimento di Scienze Biomolecolari dell'Università degli Studi di Urbino “Carlo Bo”, essendo

risultato vincitore di pubblico concorso per titoli ed esami.

Il Prof. Mantellini è stato relatore di diverse tesi di Laurea Magistrali e tesi di Dottorato in Scienze

Chimiche, ed ha partecipato a numerose commissioni di Laurea per i Corsi in Chimica e Tecnologie

Farmaceutiche, Farmacia, Biotecnologie, Biologia, Restauro e Conservazione dei Beni Culturali.

Il Prof. Mantellini ha allacciato contatti con diverse realtà nazionali ed internazionali per il

reperimento di fondi per la ricerca che hanno portato a collaborazioni con Du-Pont USA, Merck-

Serono, Syngenta AG, Gruppo Paci Pagliari, Società Aesis Therapeutics.

Il Prof. Mantellini è autore di 85 pubblicazioni scientifiche ad alto fattore di impatto su riviste

internazionali e di 54 comunicazioni a convegni nazionali ed internazionali.

ELENCO DELLE PUBBLICAZIONI

1) O. A. Attanasi, P. Filippone, C. Fiorucci, F. Mantellini, "1-Amino-2-chloromethylene -2,3-

dihydropyrroles by unusual reaction of conjugated azoalkenes with 2-chloro-1,3-dicarbonyl

compounds.", Tetrahedron Letters, 1997, 38, 873. (Q1)

2) O. A. Attanasi, P. Filippone, C. Fiorucci, F. Mantellini, "Synthesis and reactions of some 4-chloro-4-

alkoxycarbonyl-1,2-diaza-1,3-butadienes.", Gazzetta Chimica Italiana, 1997, 127, 201.

3) O. A. Attanasi, P. Filippone, C. Fiorucci, F. Mantellini, "Novel and convenient synthesis of 1,4-

dihydropyridazines and pyridazines from conjugated azoalkenes.", Synlett, 1997, 1361. (Q1)

4) O. A. Attanasi, P. Filippone, C. Fiorucci, E. Foresti, F. Mantellini, "Reaction of some 1,2-diaza-1,3-

butadienes with activated methine compounds. A straightforward entry to 1,4-dihydropyridazine,

pyridazine, and 4,5(4H,5H)-cyclopropylpyrazole derivatives.", Journal of Organic Chemistry, 1998,

63, 9880. (Q1)

5) O. A. Attanasi, L. De Crescentini, P. Filippone, G. Gatti, F. Mantellini, S. Santeusanio, "Chemo-,

regio- and stereoselectivity in the olefination of hydrazone 1,4-adducts between conjugated

azoalkenes and sulphur co-activated methylene compounds.", Tetrahedron, 1998, 54, 7581. (Q2)

6) O. A. Attanasi, P. Filippone, C. Fiorucci, F. Mantellini, "Aspects of the chemistry of functionalized

1-phenylpyrazoles available from 1,2-diaza-1,3-butadienes and 2-phenylazo-1,3-dicarbonyl

compounds.", Tetrahedron Letters, 1999, 40, 3891. (Q2)

7) O. A. Attanasi, R. Ballini, L. De Crescentini, P. Filippone, F. Mantellini, "Easy access to (E,Z)--

nitro---olefinated hydrazones, 6-oxo-1,6-dihydropyridazines, and 4-chloro-1-aminopyrroles by

domino reactions of 1,2-diaza-1,3-butadienes with halogen-coactivated methylene or methine

compounds.", Journal of Organic Chemistry, 1999, 64, 9653. (Q1)

8) O. A. Attanasi, P. Filippone, B. Guidi, C. Fiorucci, F. Mantellini, L. F. Tietze , "First preparation and

reaction of polymer-bound 1,2-diaza-1,3-butadienes. A convenient entry to 4-

triphenylphosphoranilidene-4,5-dihydropyrazol-5-ones.", Tetrahedron Letters, 1999, 40, 9277. (Q2)

9) O. A. Attanasi, P. Filippone, C. Fiorucci, F. Mantellini, “Reaction between conjugated azoalkenes

and pyrazolinones: a precious entry to new conjugated azodiene and asymmetric 4,4'-bipyrazole

derivatives.”, Chem . Lett., 2000, 984. (Q1)

10) O. A. Attanasi, L. De Crescentini, P. Filippone, E. Foresti, F. Mantellini, "2-Oxohydrazones, 4-

Hydrazono-1H-pyrazol-5-ones, and derived products by air oxidation of 1,2-hydrazino-hydrazones.",

Journal of Organic Chemistry, 2000, 65, 2820. (Q1)

11) O. A. Attanasi, L. De Crescentini, P. Filippone, F. Mantellini, "Easy synthesis of new 2-oxo-2,3-

dihydro-1H-pyrrolo[1,2-b]pyrazole systems.", Synlett, 2000, 955. (Q1)

12) O. A. Attanasi, L. De Crescentini, P. Filippone, F. Fringuelli, F. Mantellini, M. Matteucci, O.

Piermatti, F. Pizzo, "Inverse electron-demand Diels-Alder reactions of (E)-3-diazenylbut-2-enes in

water.", Helvetica Chimica Acta, 2001, 84, 513. (Q1)

13) O. A. Attanasi, L. De Crescentini, P. Filippone, F. Mantellini, "Double 1,4-addition of malonate to

1,2-diaza-1,3-butadienes: a useful route to previously unknown symmetric and unsymmetric 1,6-

dioxo-2,7-diazaspiro[4.4]nona-3,8-dienes.", New Journal of Chemistry, 2001, 25, 534. (Q1)

14) O. A. Attanasi, L. De Crescentini, P. Filippone, F. Mantellini, "Straightforward entry to new 4-

substituted-1,2,3-thiadiazoles from 1,2-diaza-1,3-butadienes via Hurd-Mori reaction.", Synlett, 2001,

557. (Q1)

15) O. A. Attanasi, L. De Crescentini, P. Filippone, F. Mantellini, L. F. Tietze, "Solid-phase synthesis of

triphenylphosphoranylidene-4,5-dihydropyrazol-5-ones, 4-aminocarbonyl-pyrroles, 4-methoxy-1H-

pyrazol-5(2H)-ones and 1,2-thiazolin-4-ones from polymer-bound 1,2-diaza-1,3-butadienes.",

Tetrahedron, 2001, 57, 5855. (Q2)

16) O. A. Attanasi, L. De Crescentini, P. Filippone, F. Mantellini, S. Santeusanio, "A new convenient

liquid- and solid-phase synthesis of quinoxalines from (E)-3-diazenylbut-2-enes", Helvetica Chimica

Acta, 2001, 84, 2379. (Q1)

17) O. A. Attanasi, P. Filippone, B. Guidi, F. Mantellini, S. Santeusanio, "Regioselective synthesis of

stable 2-(trifluoromethyl)-2,3-dihydro-1H-pyrrol-2ols and derived fluorinated heterocycles.",

Synthesis, 2001, 1837. (Q2)

18) O. A. Attanasi, L. De Crescentini, G. Favi, P. Filippone, F. Mantellini, S. Santeusanio, "Eclectic 1-

aryl-1,2-diaza-1,3-butadienes: valuable tools for the preparation of pyrrol-2-ones, 1-arylpyrazoles,

2,(3-oxopyrazol-4-yl)malonates and 4-(2-oxopyrrol-3-yl)-pyrazol-3-ones.", Synthesis, 2002, 1546.

(Q2)

19) O. A. Attanasi, L. De Crescentini, G. Favi, P. Filippone, F. Mantellini, S. Santeusanio,

"Straightforward entry into 5-hydroxy-1-aminopyrrolines and the corresponding pyrroles from 1,2-

diaza-1,3-butadienes." Journal of Organic Chemistry, 2002, 67, 8178. (Q1)

20) O. A. Attanasi, L. De Crescentini, P. Filippone, F. Mantellini, S. Santeusanio, "1,2-Diaza-1,3-

butadienes: just a nice class of compounds, or powerful tools in organic chemistry? Reviewing an

experience." Arkivoc, 2002 , xi, 274.

21) O. A. Attanasi, L. De Crescentini, G. Favi, P. Filippone, G. Giorgi, F. Mantellini, S. Santeusanio,

"Expeditious synthesis of new 1,2,3-thiadiazoles and 1,2,3-selenadiazoles from 1,2-diaza-1,3-

butadienes via Hurd-Mori reactions." Journal of Organic Chemistry, 2003, 68, 1947. (Q1)

22) O. A. Attanasi, L. De Crescentini, P. Filippone, F. Mantellini*, S. Santeusanio, "Improved synthesis

of substituted quinoxaline from new N=N polymer-bound 1,2-diaza-1,3-butadienes." Synlett, 2003,

1183. (Q1)

23) O. A. Attanasi, L. De Crescentini, G. Favi, P. Filippone, F. Mantellini, S. Santeusanio, "Expeditious

synthesis of 1,2-diamino-imidazole under solvent-free conditions." Synlett, 2004, 549. (Q1)

24) O. A. Attanasi, L. De Crescentini, G. Favi, P. Filippone, F. Mantellini*, S. Santeusanio, "Access to

new 2-oxo-furo[2,3-b]pyrroles and 2-methylenepyrroles through the reaction of 1,2-diaza-1,3-

butadienes and ketoesters." Journal of Organic Chemistry, 2004, 69, 2686. (Q1)

25) O. A. Attanasi, G. Baccolini, C. Boga, L. De Crescentini, P. Filippone, F. Mantellini*, "Solvent-free

reaction of some 1,2-diaza-1,3-butadienes with phosphites: environmentally friendly access to new

diazaphospholes and E-hydrazonophosphonates." Journal of Organic Chemistry, 2005, 70, 4033.

(Q1)

26) O. A. Attanasi, L. De Crescentini, G. Favi, P. Filippone, S. Lillini, F. Mantellini, S. Santeusanio,

"Different behavior of the reaction between 1,2-diaza-1,3-butadienes and 1,2-diamines under

solvent-free conditions." Synlett, 2005, 1474. (Q1)

27) O. A. Attanasi, L. De Crescentini, G. Favi, P. Filippone, S. Lillini, F. Mantellini*, S. Santeusanio,

"Efficient synthesis and environmentally friendly reactions of PEG-supported 1,2-diaza-1,3-

butadiene." Org. Lett., 2005, 7, 2469. (Q1)

28) D. Aparicio, O. A. Attanasi, P. Filippone, R. Ignacio, S. Lillini, F. Mantellini, F. Palacios, J. M. de

los Santos, "Straightforward access to pyrazines, piperazinones, and quinoxalines by reaction of 1,2-

diaza-1,3-butadienes with 1,2-diamines under solution, solvent free, or solid-phase conditions."

Journal of Organic Chemistry, 2006, 71, 5897. (Q1)

29) O. A. Attanasi, L. De Crescentini P. Filippone, F. Mantellini, F. R. Perrulli, S. Santeusanio, "An

alternative route to pyrrolotriazoles and other N-bridgehead heterocycles." Synlett, 2006, 1734. (Q2)

30) O. A. Attanasi, L. De Crescentini, P. Filippone, G. Giorgi, F. Mantellini, A. Mazzanti, "Unusual

peptidomimetic reaction of 1,2-diaza-1,3-butadienes: straightforward entry to 2,3,6-

triazabicyclo[3.2.1]oct-3-enes, 5-oxo-4,5-dihydro-2-pyrazines, and 2-carbonyl-

oxopropylaminoacetates." Synlett, 2006, 2403. (Q2)

31) O. A. Attanasi, G. Favi, P. Filippone, G. Giorgi, S. Lillini, F. Mantellini, F. R. Perrulli, "Unexpected

ring closure between hydrazono and nitro groups: a useful synthesis of substituted pyrazole N-

oxides." Synlett, 2006, 2731. (Q2)

32) O. A. Attanasi, L. De Crescentini, G. Favi, P. Filippone, A. Golobic, S. Lillini, F. Mantellini*,

"Facile Synthesis of new substituted tetrahydro-1H-indoles." Synlett, 2006, 2735. (Q2)

33) O. A. Attanasi, S. Berretta, L. De Crescentini, G. Favi, P. Filippone, G. Giorgi, S. Lillini, F.

Mantellini*, “ Unexpected regioselectivity in the reaction between cycloalkenyl-1-diazenes and

thioamides: useful entry to fused cycloalkyl-thiazoline and cycloalkyl-thiazoline-pyrazole systems.”

Tetrahedron Letters, 2007, 48, 2449. (Q2)

34) O. A. Attanasi, G. Favi, P. Filippone, S. Lillini, F. Mantellini, D. Spinelli, M. Stenta, “ Improved

synthesis of pyrroles and indoles via Lewis acid-catalyzed Mukaiyama-Michael-type

addition/heterocyclization of enolsilyl derivatives on 1,2-diaza-1,3-butadienes. Role of the catalyst in

the reaction mechanism.” Adv. Synth. Catal., 2007, 349, 907. (Q1)

35) Schmidt, V. Karapetyan, O. A. Attanasi, G. Favi, H. Gorls, F. Mantellini, P. Langer, "Regioselective

synthesis of new 1-aminopyrroles and 1-amino-4,5,6,7-tetrahydroindoles by one-pot „conjugate

addition/cyclization‟ reactions of 1,3-bis(silyl enol ethers) with 1,2-diaza-1,3-butadienes." Synlett,

2007, 2965. (Q2)

36) O. A. Attanasi, L. De Crescentini, G. Favi, P. Filippone, G. Giorgi, F. Mantellini*, F. R. Perrulli and

D. Spinelli, "Simple construction of fused and spiro nitrogen/sulfur containing heterocycles by

addition of thioamides or thioureas on cycloalkenyl-diazenes: examples of click chemistry.",

Tetrahedron, 2008, 64, 3837. (Q2)

37) V. Karapetyan, S. Mkrtchyan, A. Schmidt, O. A. Attanasi, G. Favi, F. Mantellini, A. Villinger, C.

Fischer and P. Langer, "Diversity-oriented synthesis of functionalized 1-aminopyrroles by

regioselective ZnCl2-catalyzed one-Pot conjugate addition/cyclization reactions of 1,3-bis(silyl

enol ethers) with 1,2-diaza-1,3-butadienes.", Advanced Synthesis & Catalysis, 2008, 350, 1331. (Q1)

38) O. A. Attanasi, G. Favi, P. Filippone, G. Giorgi, F. Mantellini, G. Moscatelli and D. Spinelli,

"Flexible protocol for the chemo- and regioselective building of pyrroles and pyrazoles by reactions

of Danishefsky‟s dienes with 1,2-diaza-1,3-butadienes.", Organic Letters, 2008, 10, 1983. (Q1)

39) O. A. Attanasi, G. Favi, P. Filippone, G. Giorgi, F. Mantellini, G. Moscatelli and D. Spinelli,

"Synthesis of pyrroles and pyrazoles by Mukaiyama-Michael addition/heterocyclization.", Synfacts,

2008, 8, 801.

40) O. A. Attanasi, G. Baccolini, C. Boga, L. De Crescentini, P. Filippone and F. Mantellini, "Carbon-

phosphorus bond formation and transformation in the reaction of 1,2-diaza-1,3-butadienes with alkyl

phenylphosphonites.", Tetrahedron, 2008, 64, 6724. (Q2)

41) O. A. Attanasi, P. Filippone, S. Lillini, S. Nicolini, F. Mantellini, D. Aparicio, R. Ignacio, J. M. de

los Santos and F. Palacios, "Reactions of 1,2-diaza-1,3-dienes with thiol derivatives: a versatile

construction of nitrogen/sulfur containing heterocycles.", Tetrahedron, 2008, 64, 9264. (Q2)

42) L. Forlani, O. A. Attanasi, C. Boga, L. De Crescentini, E. Del Vecchio, G. Favi, F. Mantellini, S.

Tozzi and N. Zanna, "Unusual reaction between aromatic carbon supernucleophiles and 1,2-diaza-

1,3-butadienes. Useful entry to new pyrazolone and cinnoline derivatives.", European Journal of

Organic Chemistry, 2008, 4357. (Q1)

43) O. A. Attanasi, M. D‟Auria, L. Emanuele, G. Favi, P. Filippone, F. Mantellini, R. Pucciarello and R.

Racioppi, "Synthesis of new polyazines by 1,4 photochemical or anionic polymerization of 1,2-

diaza-1,3-dienes.", European Polymer Journal, 2008, 44, 2545. (Q1)

44) O. A. Attanasi, G. Baccolini, C. Boga, L. De Crescentini, G. Giorgi, F. Mantellini and S. Nicolini,

"Reaction of 1,2-diaza-1,3-butadienes with amino-phosphorus nucleophiles: a pratical access to new

phosphorylated-pyrazolones.", European Journal of Organic Chemistry, 2008, 5965. (Q1)

45) O. A. Attanasi, S. Berretta, L. De Crescentini, G. Favi, A. Golobic and F. Mantellini*, "Synthesis of

new cycloalkenyliden-pyrroles by domino reaction.", Tetrahedron, 2009, 65, 2290. (Q1)

46) O. A. Attanasi, S. Lillini, F. Mantellini*, J. M. de los Santos, R. Ignacio and F. Palacios, "Domino

reaction for the construction of new 2-oxo-[1,2,4]triazolo[5,1-c][1,4]thiazines.", Synlett, 2009, 735.

(Q2)

47) O. A. Attanasi, L. De Crescentini, F. Mantellini, F. Marini, S. Nicolini, S. Sternativo and M. Tiecco,

"Easy synthesis of selenium-substituted pyrroles and pyrazol-3-ones.", Synlett, 2009, 1118. (Q2)

48) O. A. Attanasi, S. Berretta, L. De Crescentini, G. Favi, G. Giorgi and F. Mantellini*, "Lewis acid-

catalyzed synthesis of functionalized pyrroles.", Advanced Synthesis & Catalysis, 2009, 351, 715.

(Q1)

49) O. A. Attanasi, L. De Crescentini, G. Favi, P. Filippone, G. Giorgi, F. Mantellini, G. Moscatelli and

M. S. Behalo, "An efficient one-pot, three-component synthesis of 5-hydrazinoalkylidene rhodanines

from 1,2-diaza-1,3-dienes.", Organic Letters, 2009, 11, 2265. (Q1)

50) O. A. Attanasi, G. Favi, G. Giorgi, F. Mantellini, V. Karapetyan and P. Langer, "Regioselective

synthesis of spiro-cyclopropanated 1-aminopyrrol-2-ones by Bi(OTf)3-catalyzed one-pot

„Mukaiyama-Michael addition/cyclization/ring-contraction‟ reactions of 1,2-

bis(trimethylsilyloxy)cyclobutene with 1,2-diaza-1,3-butadienes.", Tetrahedron, 2009, 65, 5456.

(Q1)

51) O. A. Attanasi, L. De Crescentini, G. Favi, P. Filippone, F. Mantellini, F. R. Perrulli and S.

Santeusanio, "Cultivating the passion to build heterocycles from 1,2-diaza-1,3-dienes: the force of

the imagination.", European Journal of Organic Chemistry, 2009, 3109. (Q2)

52) O. A. Attanasi, E. Caselli, P. Davoli, G. Favi, F. Mantellini, C. Ori and F. Prati, "alpha-Aminoester-

derived imidazoles by 1,5-electrocyclization of azavinyl azomethine ilides.", Organic Letters, 2009,

11, 2840. (Q1)

53) O. A. Attanasi, G. Favi, P. Filippone, F. Mantellini, G. Moscatelli, F. R. Perrulli,

"Copper(II)/Copper(I)-catalyzed aza-Michael addition/click reaction of in situ generated -

azidohydrazones: synthesis of novel pyrazolone-triazole framework.", Organic Letters, 2010, 12,

468. (Q1)

54) G. Pitacco, O. A. Attanasi, L. De Crescentini, G. Favi, F. Felluga, C. Forzato, F. Mantellini, P. Nitti,

E. Valentin and E. Zangrando, "Organocatalysed synthesis of chiral non racemic 1,4-

dihydropyridazines.", Tetrahedron: Asymmetry, 2010, 21, 617. (Q2)

55) M. D‟Auria, R. Racioppi, O. A. Attanasi and F. Mantellini, "Unusual (4+2)-cycloaddition reaction

between electron poor 1,2-diaza-1,3-dienes and electron poor alkenes: useful entry to novel

tetrahydropyridazines.", Synlett, 2010, 1363. (Q1)

56) O. A. Attanasi, S. Bartoccini, G. Giorgi, F. Mantellini,

F. R. Perrulli and S. Santeusanio "Study of the

nucleophilic behaviour of N-phenylbenzamidine towards 1,2-diaza-1,3-dienes: domino reactions for

imidazole scaffolds.", Tetrahedron, 2010, 66, 5121. (Q2)

57) O. A. Attanasi, S. Berretta, L. De Crescentini, G Favi, P. Filippone, G. Giorgi and F. Mantellini*,

"Divergent base-induced reactivity of cycloalkenyl-1-diazenes.", Tetrahedron, 2010, 66, 6832. (Q2)

58) C. Boga, N. Zanna, O. A. Attanasi, G. Baccolini, L. De Crescentini, L. Forlani, F. Mantellini, S.

Nicolini, G. Micheletti and S. Tozzi, "Phospha-Michael-type reaction between 1,2-diaza-1,3-dienes

and bidentate nucleophiles. formation of new mono- and diylides and their elaboration to

heterocycles.", European Journal of Organic Chemistry, 2011, 1326. (Q2)

59) O. A. Attanasi, S. Berretta, L. De Crescentini, G. Favi, G. Giorgi, F. Mantellini* and S. Nicolini,

"Zinc(II) triflate catalyzed divergent synthesis of polyfunctionalized pyrroles.", Advanced Synthesis

& Catalysis, 2011, 353, 595. (Q1)

60) O. A. Attanasi, G. Favi, F. Mantellini, G. Moscatelli and S. Santeusanio, "Synthesis of functionalized

pyrroles via catalyst- and solvent-free sequential three-component enamine-azoene annulation.",

Journal of Organic Chemistry, 2011, 76, 2860. (Q1)

61) O. A. Attanasi, G. Favi, F. Mantellini, G. Moscatelli and S. Santeusanio, "A novel assembly of

substituted pyrroles by acid-catalyzed sequential three–component reaction of amines, alkynoates,

and 1,2-diaza-1,3-dienes.", Advanced Synthesis & Catalysis, 2011, 353, 1519. (Q1)

62) O. A. Attanasi, L. Bianchi, L. De Crescentini, G. Favi and F. Mantellini*, "Easy one-pot synthesis of

fused heterocycles from 1,2-diaza-1,3-dienes.", European Journal of Organic Chemistry, 2011,

2924. (Q2)

63) O. A. Attanasi, S. Berretta, L. De Crescentini, G. Favi, G. Giorgi, F. Mantellini* and S. Nicolini,

"Zinc(II) triflate catalyzed divergent synthesis of polyfunctionalized pyrroles.", Synfacts, 2011, 605.

64) O. A. Attanasi, L. De Crescentini, G. Favi, F. Mantellini and S. Nicolini, “Divergent Regioselective

Synthesis of 2,5,6,7-Tetrahydro-1H-1,4-diazepin-2-ones and 5H-1,4-Benzodiazepines.”, Journal of

Organic Chemistry, 2011, 76, 8320. (Q1)

65) O. A. Attanasi, G. Favi, F. Mantellini, S. Menichetti, G. Moscatelli and C. Viglianisi, “Synthesis of

highly functionalized 1,3-oxathioles via an unusual [4+1] annulation of ‟-dioxothione with 1,2-

diaza-1,3-dienes.”, Synlett, 2012, 2947. (Q2)

66) O. A. Attanasi, L. Bianchi, J. Bezensek, G. Favi, G. Giorgi, F. Mantellini*, B. Stanovnik and J.

Svete, “Divergent behaviour of the reactions between 1,2-diaza-1,3-dienes and 2,5-

dioxoimidazolidin-4-ylidene-succinates.”, Current Organic Synthesis, 2013, 10, 472 (2013). (Q2)

67) O. A. Attanasi, G. Favi, A. Geronikaki, F. Mantellini, G. Moscatelli and A. Paparisva, “Synthesis of

densely functionalized 3a,4-dihydro-1H-pyrrolo[1,2-b]pyrazoles via base mediated domino reaction

of vinyl malonitriles with 1,2-diaza-1,3-dienes.”, Organic Letters, 2013, 15, 2624. (Q1)

68) O. A. Attanasi, l. Bianchi, L. A. Campisi, L. De Crescentini, G. Favi, and F. Mantellini*, “A Novel

Solvent-Free Approach Containing Nitrogen-Bridgehead Heterocycles.”, Organic Letters, 15, 3646

(2013). (Q1)

69) O. A. Attanasi, L. Bianchi, M. D‟Auria, F. Mantellini* and R. Racioppi, “Novel

tetrahydropyridazines by unusual Aza-Diels-Alder reaction of electron-poor 1,2-diaza-1,3-dienes

with electron-poor alkenes under solvent-free conditions.”, Current Organic Synthesis, 2013, 9, 631.

(Q2)

70) O. A. Attanasi, G. Favi, G. Giorgi, F. Mantellini, G. Moscatelli and G. Piersanti, “Synthesis of

tetrahydropyridazine amino acid derivatives by a formal [4+2]cycloaddition reaction of 1,2-diaza-

1,3-dienes with dehydroalanine esters.”, Current Organic Synthesis, 2013, 10, 803 (2013). (Q2)

71) O. A. Attanasi, L. Bianchi, M. D‟Auria, G. Favi, F. Mantellini* and R. Racioppi, “Aza-Diels-Alder

reaction between 1,2-diaza-1,3-dienes and -aryl--unsaturated carbonyl compounds. Easy one-

pot entry to 2‟-oxo-imidazo[1‟,5‟-f]tetrahydropyridazine.”, Current Organic Synthesis, 2013, 10,

951. (Q2)

72) O. A. Attanasi, L. De Crescentini, G. Favi, F. Mantellini, S. Mantenuto and S. Nicolini, “Interceptive

[4+1]annulation of in situgenerated 1,2-diaza-1,3-dienes with diazo esters: direct access to substituted

mono-, bi-, and tricyclic 4,5-dihydropyrazoles.”, Journal of Organic Chemistry, 2014, 79, 8331. (Q1)

73) O. A. Attanasi, L. A. Campisi, L. De Crescentini, G. Favi, F. Mantellini*, “Synthesis of novel

symmetrical 2-oxo-spiro[indole-3,4‟-pyridines] by reaction of oxindoles with 1,2-diaza-1,3-dienes”,

Organic Biomolecular Chemistry, 2015, 13, 277. (Q1).

74) O. A. Attanasi, G. Favi, F. Mantellini, S. Mantenuto, G. Moscatelli, S. Nicolini “Regioselective

Formation of 5-methylene-1,4,5,6-tetrahydropyridazines from the [4+2] cycloaddition reaction of in

situ-generated 1,2-diaza-1,3-dienes with methoxyallenes” Synlett, 2015, 193. (Q2).

75) S. Mantenuto, F. Mantellini, G. Favi, O. A. Attanasi “Divergent Construction of Pyrazoles via

Michael Addition of Arylhydrazones to 1,2-Diaza-1,3-dienes” Org. Lett, 2015, 17, 2014. (Q1).

76) L. De Crescentini, O. A. Attanasi, L. A. Campisi, G. Favi, S. Lillini, F. Ursini, F. Mantellini, “ Double

Michael addition/aza-cyclization: a valuable sequence for the construction of symmetrical and

unsymmetrical spirobarbiturate-pyridines” Tetrahedron, 2015, 61, 7282. (Q2).

77) F. R. Perrulli, G. Favi, L. De Crescentini, O. A. Attanasi, S. Santeusanio, F. Mantellini, “

Regioselective [1N+2C+2C] assembly of fully decorated pyrroles from primary amines, 1,2-diaza-1,3-

dienes, and 2,3-allenoates” European Journal of Organic Chemistry, 2015, 7154. (Q1).

78) G. Mari, G. Favi, L. De Crescentini, S. Santeusanio, O. A. Attanasi, F. Mantellini, "Facile, Odourless,

Quantitative Synthesis of 3-Hydroxy-3,4-dihydro-2H-1,4-thiazines" Asian J. Org. Chem., 2016, 5, 705

IF: 3.275; (Q2).

79) S. Mantenuto, S. Lucarini, M. De Santi, G. Piersanti, G. Brandi, G. Favi, F. Mantellini, "One-Pot

Synthesis of Novel Bi-heterocycles Based on Indole and Azole Scaffolds Using Tryptamines and 1,2-

Diaza-1,3-dienes as Building Blocks" Eur. J. Org. Chem., 2016, 3193. IF: 3.068;(Q2).

80) S. Mantenuto, A. Cayuelas, G. Favi, O. A. Attanasi, F. Mantellini, C. Nájera, J. M. Sansano,

“Reactivity of 1,2-Diaza-1,3-dienes with Azomethine Ylides: [3+4] versus [3+2] Cycloadditions” Eur.

J. Org. Chem., 2016, 4144. IF: 3.068; (Q2).

81) L. De Crescentini, F. R. Perrulli, G. Favi, S. Santeusanio, G. Giorgi, O. A. Attanasi, F. Mantellini

“Reactions of 1,2-diaza-1,3-butadienes with propargyl alcohol as approach to novel bi-heterocyclic

systems” Org. Biomol. Chem., 2016, 14, 8674. IF: 3.559; (Q1).

82) S. Mantenuto, C. Ciccolini, S. Lucarini, G. Piersanti, G. Favi, F. Mantellini, " Palladium(II)-Catalyzed

Intramolecular Oxidative C−H/C−H Cross-Coupling Reaction of C3,N-linked Biheterocycles: Rapid

Access to Polycyclic Nitrogen Heterocycles" Org. Lett., 2017, 19, 608. IF: 6.732; (Q1).

83) A. Fattori, R. Majer, A. Mazzanti, M. F. Ottaviani, A. Modelli, F. Mantellini S. Santeusanio,

“N-Heterocyclic linkers from 1,2-Diaza-1,3-dienes for dye-sensitized solar cells: DFT calculations,

synthesis and photovoltaic performance” Dyes Pigm., 2017, 145, 246. IF: 3.473; (Q1).

84) G. Mari, L. De Crescentini, G. Favi, p. Lombardi, G. Fiorillo, G. Giorgi F. Mantellini, "Heteroring

Annulated Pyrrolino-tetrahydroberberine Analogues" Asian J. Org. Chem., 2017, 6, 720 IF: 3.275;

(Q2).

85) S. Santeusanio, R. Majer, F. R. Perrulli, L. De Crescentini, G. Favi, G. Giorgi, F. Mantellini,

“Divergent Approach to Thiazolylidene derivatives: a Perspective in the Synthesis of Heterocyclic

Skeleton from -Amidothioamides Reactivity” J. Org. Chem., 2017, 0000. IF: 4.489; (Q1).

Autorizzo il trattamento dei dati personali contenuti nel mio curriculum vitae in base art. 13 del D. Lgs. 196/2003.

In fede

Fabio Mantellini