{"id":8,"date":"2015-04-08T11:14:00","date_gmt":"2015-04-08T09:14:00","guid":{"rendered":"http:\/\/people.unipi.it\/mauro_pineschi\/?page_id=8"},"modified":"2025-12-23T18:26:47","modified_gmt":"2025-12-23T17:26:47","slug":"pubblicazioni","status":"publish","type":"page","link":"https:\/\/people.unipi.it\/mauro_pineschi\/pubblicazioni\/","title":{"rendered":"Pubblicazioni"},"content":{"rendered":"\n<ul class=\"wp-block-list\">\n<li><em>Alternating Current for Electrooxidative Nitroso Diels\u2212Alder Reaction on 1,2-Dihydropyridines.<\/em><strong> <\/strong>C. Campinoti, F. M. Vivaldi, F. Sardelli, M. Pineschi, F. Di Francesco, F. Bellina,* A. Del Vecchio,* and M. Lessi. <em>J. Org. Chem.<\/em> In press https:\/\/doi.org\/10.1021\/acs.joc.5c01868.<\/li>\n\n\n\n<li><em>Synthesis and biological evaluation of N-O heterobicyclic ring systems derived from 1,2-dihydropyridines as novel TRPA1 activators: implication in GLP-1 release and neuroprotection<\/em> L. M. Comparini, V. Citi, G. Ortore, G. Daniele, F. Sardelli, G. Galgani, G. Bray, C. Filipponi, A. De Carli, M. Lai, M. Nardone, V. Calderone, M. Falasca, M. Pineschi &#8211;<em> Eur. J. Med. Chem. <\/em><strong>2025<\/strong>.<em> doi: 10.1016\/j.ejmech.2025.118115<\/em><\/li>\n\n\n\n<li><em>Synthesis of Highly Functionalized Tetrahydropyridines by Ring Opening of [3.3.1]-Heterobicyclic Compounds with Grignard Reagents.<\/em> . M. Comparini, G. Turchi, F. Sardelli, L. Favero, V. Di Bussolo, S. Di Pietro, M. Pineschi. <em>Asian J. Org. Chem.<\/em> <strong>2025<\/strong>, e202400743.<\/li>\n\n\n\n<li><em>Glycoconjugate coumarins exploiting metabolism-enhanced fluorescence and preferential uptake: New optical tools for tumor cell staining. D. Iacopini, M. Santi, M. C. Santangelo, G. Sardelli, L. Piazza, R. Mosca, L. M. Comparini, C. Granchi, M. Pineschi, S. Di Pietro, G. Signore, V. Di Bussolo<\/em>. <em>Bioorg. Chem.<\/em> <strong>2024<\/strong>, <em>153<\/em>, 107836. <a href=\"https:\/\/doi.org\/10.1016\/j.bioorg.2024.107836\">https:\/\/doi.org\/10.1016\/j.bioorg.2024.107836<\/a><\/li>\n\n\n\n<li><em>Ring-Opening Reactions of Imidazolidines and Hexahydropyrimidines with Grignard Reagents.<\/em>L. M. Comparini, G. Gallorini, L. Favero, F. Sardelli, V. Di Bussolo, S. Di Pietro, M. Pineschi. <em>J. Org. Chem.<\/em>&nbsp;<strong>2024<\/strong>,&nbsp;<em>89<\/em>,&nbsp;15652-15664.<strong>&nbsp;<\/strong><\/li>\n\n\n\n<li>Streamlined Stereoselective Entry to (-)-Quinagolide and to 3-Substituted Octahydrobenzo[g]-Quinolines<em>.<\/em> F. Sardelli, L. M. Comparini, L. Favero, S. Di Pietro, P. Ryberg, M. Pineschi. <em>J. Org. Chem.<\/em> <strong>2024<\/strong>, <em>89<\/em>, 2649-2655.<\/li>\n\n\n\n<li><em>Recent Progresses in the Catalytic Stereoselective Dearomatization of Pyridines<\/em>. L. M. Comparini, M. PIneschi. <em>Molecules <\/em><strong>2023<\/strong>, <em>28<\/em>, 6186. <a href=\"https:\/\/doi.org\/10.3390\/molecules28176186\">https:\/\/doi.org\/10.3390\/molecules28176186<\/a>Development of an asymmetric formal synthesis of (\u2212)-quinagolide via enzymatic resolution and stereoselective iminium ion reduction L. M. Comparini, &nbsp;A. Menichetti, L. Favero,&nbsp;S. Di Pietro, F. Badalassi,&nbsp; P. Ryberg &nbsp;and M. Pineschi, <em>Org. Biomol. Chem<\/em>. <strong>2023<\/strong>, <em>21<\/em>, 6389\u20136396.<\/li>\n\n\n\n<li>Recent Progresses in the Catalytic Stereoselective Dearomatization of Pyridines. L. M. Comparini, M. Pineschi <em>Molecules <\/em><strong>2023<\/strong>, <em>28<\/em>, 6186. https:\/\/doi.org\/10.3390\/molecules28176186.<\/li>\n\n\n\n<li><em>Boron Reagents and Catalysts for the Functionalization of Strained Heterocycles<\/em>. M. Pineschi, <em>Adv. Synth. Catal. <strong>2021<\/strong>, 363, 2325-2339.<\/em><strong> DOI:&nbsp;<\/strong>10.1002\/adsc.202001493 (<strong>Very Important Paper<\/strong>)&nbsp; <\/li>\n\n\n\n<li><em>New 1,3-disubstituted benzo[h]isoquinoline cyclen-based ligand platform: Synthesis, Eu<sup>3+<\/sup>multiphoton sensitization and imaging applications<\/em>. S. Di Pietro, D. Iacopini, B. Storti, R. Nifos\u00ec, V. Di Bussolo, M. Pineschi, A. Moscardini, G. Signore, R. Bizzarri, <em>Molecules <\/em><strong>2021<\/strong>, <em>26<\/em>, 58. hdl:11568\/1068767<\/li>\n\n\n\n<li><em>New lipophilic glycomimetic DC-SIGN ligands: Stereoselective synthesis and SPR-based binding inhibition assays<\/em>. S. Di Pietro, V. Bordoni, D. Iacopini, S. Achilli, M. Pineschi, M. Th\u00e9paut, F. Fieschi, P. Crotti, V. Di Bussolo, <em>Bioorganic Chemistry<\/em> <strong>2021<\/strong>, <em>107<\/em>, 104566. <\/li>\n\n\n\n<li><em>Experimental   and Computational Studies Unraveling the Peculiarity of Enolizable Oxoesters   in the Organocatalyzed Mannich-Type Addition to Cyclic N-Acyl Iminium Ions <\/em>   Menichetti,   S. Di Pietro, V. Di Bussolo, L. Favero, M. Pineschi      <em>Molecules<\/em>&nbsp;<strong>2020<\/strong>,&nbsp;<em>25<\/em>, 1903.   &nbsp;         <\/li>\n\n\n\n<li><em>The   Binomial Copper-Catalysis and Asymmetric Ring Opening of Strained   Heterocycles: Past and Future Challenges<\/em>.   &nbsp;   M. Pineschi   &nbsp;   <em>Eur.   J. Org. Chem.<\/em> <strong>2020<\/strong>,    2643-2649 (<strong>Very Important Paper<\/strong>)&nbsp; <\/li>\n\n\n\n<li><em>Nitroso Diels-Alder   Cycloadducts Derived from N-Acyl-1,2-dihydropyridines as a New Platform to   Molecular Diversity<\/em>      A. Menichetti, F.   Berti, M. Pineschi, <em>Molecules<\/em>&nbsp;<strong>2020<\/strong>,&nbsp;<em>25<\/em>(3), 563.  <\/li>\n\n\n\n<li>M. Pineschi, C. Boldrini, In <em>Science of Synthesis: Advances in Organoboron Chemistry towards Organic Synthesis<\/em>, (Eds.: E. Fern\u00e1ndez), Thieme: Stuttgart, <strong>2020<\/strong>, &nbsp;pp.183-22. &nbsp;   <\/li>\n\n\n\n<li>  Enantiopure cis- and trans-2,5-disubstituted-2,5-dihydrofurans from D-allal- and D-galactal-derived vinyl epoxides<a href=\"https:\/\/www.scopus.com\/record\/display.uri?eid=2-s2.0-85068118157&amp;origin=resultslist&amp;sort=plf-f&amp;src=s&amp;st1=pineschi&amp;st2=mauro&amp;nlo=1&amp;nlr=20&amp;nls=afprfnm-t&amp;sid=4ba1e5daa411408d622f1c681ed03c6c&amp;sot=anl&amp;sdt=aut&amp;sl=35&amp;s=AU-ID%28%22Pineschi%2c+Mauro%22+7004740686%29&amp;relpos=1&amp;citeCnt=0&amp;searchTerm=\">.<\/a>  V.   Di Bussolo et al.   <em>Tetrahedron   <\/em><strong>2019<\/strong>, <em>75<\/em>, 4425-4443.     <\/li>\n\n\n\n<li> <em>Direct   Enantioselective Vinylogous Mannich-type Reactions of Acyclic Enals: New   Experimental Insights into the E\/Z-Dilemma<\/em>   M. Vargiu, L. Favero, A. Menichetti,V.   Di Bussolo, F. Marchetti,G. Pescitelli,S. Di Pietro,  M. Pineschi <em> Chirality<\/em> <strong>2019<\/strong>, 31, 522-533.      <\/li>\n\n\n\n<li>   <em>Organocatalytic alkylation of   carbohydrate\u2010containing aldehydes with dihydroquinoline N,O\u2010acetals:   Absolute configuration of 1,2\u2010dihydroquinolines<\/em>.  A. Menichetti, F. Berti, L. Guazzelli,   L. Favero, S. Di Pietro, G. Pescitelli, M. &nbsp;Pineschi,  <em>Chirality <\/em><strong>2019<\/strong>,   <em>31<\/em>, 127\u2013137. &nbsp;  <\/li>\n\n\n\n<li> &nbsp;<em>Regio- and Stereodivergent Allylic Reductions of   Bicyclic Piperidine Enecarbamate Derivatives<\/em>   F. Berti, A. Menichetti,L. Favero, F. Marchetti, M. Pineschi,   <em>J. Org. Chem. <strong>2018<\/strong>, 83, 12221-12228.<\/em>  <\/li>\n\n\n\n<li>   <em>Synthesis of bicyclic tetrahydropyridine enamides   and enecarbamates by hetero-Cope rearrangement of nitroso cycloadducts<\/em>   F. Berti, A. Menichetti, V. Di Bussolo, L. Favero, M. Pineschi, <em>Chem. Heter. Comp. <strong>2018<\/strong>, 54, 458-468.<\/em>         <\/li>\n\n\n\n<li><em>Asymmetric   Synthesis of Methylphenidate and Quinolizidinones by Addition of Aldehydes to   Piperidine-Based Conjugated N-Acyl Iminium Ions<\/em>   F.   Berti, L. Favero, M. Pineschi,   <em>Synthesis<\/em> <strong>2016<\/strong>, <em>48<\/em>,   2645-2652.   <\/li>\n\n\n\n<li><em>Highly enantioselective Mannich   reaction of aldehydes with cyclic N-acyliminium ions by synergistic catalysis<\/em>   F.   Berti, F. Malossi, F. Marchetti, M. Pineschi,  <em>Chem. Commun. <\/em><strong>2015<\/strong><em>, 51<\/em>, 13694 \u201313697.<\/li>\n\n\n\n<li>   <em>Synthesis of   2,7-Diazabicyclo[2.2.1]-heptenes by N-O Bond&nbsp;   Cleavage of Arylnitroso Diels-Alder 1,2-Dihydropyridine-Cycloadducts<\/em>   F.   Berti, V. Di Bussolo, M. Pineschi   <em>Synthesis<\/em> <strong>2015<\/strong>,   <em>47<\/em>, 647-652.   &nbsp;    <\/li>\n\n\n\n<li>  <a href=\"http:\/\/unimap.unipi.it\/cercapersone\/prodottodett.php?idpr=559868&amp;iddoc=009021\"><em>Advances in the Ring Opening of   Small-Ring Heterocycles with Organoboron Derivatives<\/em><\/a>   M. Pineschi   <em>Synlett<\/em> <strong>2014<\/strong>, <em>25<\/em>, 1817-1826.  <\/li>\n\n\n\n<li> &nbsp;  <em>Enantiopure Cis-2,5-Disubstituted   2,5-Dihydropyrroles from d-Glycal-Derived Vinyl Aziridines<\/em>   V. Di Bussolo, I.   Frau, S. Crotti, G. Uccello-Barretta, F. Balzano, M. Pineschi, P. Crotti   <em>Org. Lett.<\/em> <strong>2013<\/strong>, <em>15<\/em>, 6026-6029.   &nbsp;      <\/li>\n\n\n\n<li><em>Synthesis   of Protected (1-Phenyl\u20111H\u2011pyrrol-2-yl)-alkane-1-amines from Phenylnitroso   Diels\u2212Alder Adducts with 1,2-Dihydropyridines<\/em>   F. Berti, V. Di Bussolo, M. Pineschi   <em>J. Org. Chem.<\/em> <strong>2013<\/strong>,   <em>78<\/em>, 7324-7329. <\/li>\n\n\n\n<li>  <em>Regio- and   Stereoselective Ring Opening of Allylic Epoxides<\/em>   Pineschi, M. Bertolini, F.; Di Bussolo, V.; Crotti, P.   <em>Advances in   Organic Synthesis, <\/em><strong>2013<\/strong><em>, 5, <\/em>101-184.   &nbsp;    <\/li>\n\n\n\n<li>  <em>Copper-Catalyzed   Arylation of Alkenyl Aziridines via Three-Component Coupling Reaction   involving Alkynes and Benzyne<\/em>   F. Berti, P. Crotti, G. Cassano, M. Pineschi   <em>Synlett <\/em><strong>2012<\/strong>, <em>23<\/em>, 2463-2468.   <\/li>\n\n\n\n<li>&nbsp;  <em>Stereoselective   Ring Opening of Bicyclic Nitroso Diels-Alder Cycloadducts with Carbon   Nucleophiles <\/em>   S. Crotti, M. Pineschi   <em>Curr. Org. Synth<\/em>. <strong>2012<\/strong>, <em>9<\/em>, 460-469.   &nbsp;      <\/li>\n\n\n\n<li><em>Synthesis   D-Allal- and D-Galactal-Derived Vinyl N-Mesylaziridines:   Regio- and Stereoselectivity in Addition Reactions of O-, C-, N-, and   S-Nucleophiles<\/em>   V. Di Bussolo, I. Frau, M. Pineschi, P. Crotti   <em>Synthesis<\/em> <strong>2012<\/strong>,   2863.   &nbsp;      <\/li>\n\n\n\n<li><em>Regio- and   Stereoselective Copper-Catalyzed Ring Opening of Diheterobicyclic Alkenes   with Grignard Reagents<\/em>   S. Crotti, V. Di Bussolo, M. Pineschi   <em>Synthesis<\/em> <strong>2012<\/strong>,   1511.   &nbsp;      <\/li>\n\n\n\n<li><em>Copper-Catalyzed   Perkin Acyl-Mannich Reaction of Acetic Anhydride with Pyridine: Expeditious   Entry to Unconventional Piperidines<\/em>   S. Crotti, F. Berti, M. Pineschi   <em>Org. Lett.<\/em> <strong>2011<\/strong>, <em>13<\/em>, 5152-5155.   &nbsp; <\/li>\n\n\n\n<li> <em>Stereodivergent Synthesis of Diastereoisomeric Carba Analogs of   Glycal-Derived Vinyl Epoxides: A New Access to Carbasugars<\/em>   I. Frau, V. Di Bussolo, L. Bavero, M. Pineschi, P.   Crotti   <em>Chirality <\/em><strong>2011<\/strong>, <em>23<\/em>, 820-826.   &nbsp;      <\/li>\n\n\n\n<li><em>Copper-Catalyzed Divergent Kinetic Resolution of Racemic Allylic   Substrates <\/em>   M. Pineschi, V. Di Bussolo, P. Crotti   <em>Chirality<\/em> <strong>2011<\/strong>, <em>23<\/em>, 703-710.<\/li>\n\n\n\n<li><em>Synthesis of   carba analogs of 6-O-(benzyl)-D-allal- and -D-galactal-derived allyl epoxides   and evaluation of the regio- and stereoselective behavior in nucleophilic   addition reactions<\/em>   V. Di Bussolo, I. Frau, L. Checchia, L. Favero, M. Pineschi, G.   Uccello-Barretta, F. Balzano, G. Roselli, G. Renzi, P. Crotti   <em>Tetrahedron<\/em> <strong><em>2011<\/em><\/strong>, <em>67<\/em>, 4696-4709.   <\/li>\n\n\n\n<li>&nbsp;<em>BACE1 inhibitory activity   of enantiomerically pure, variously substituted   N-(3-(4-benzhydrylpiperazin-1-yl)-2-hydroxypropyl) arylsulfonamides<\/em>   S. Bertini, E. Ghilardi, V. Asso, C. Granchi, F. Minutolo, M. Pineschi,   V. Di Bussolo, A. Bortolato, S. Moro, A. Saba, M. Macchia   <em>Biorg. Med. Chem.<\/em> <strong>2010<\/strong>, <em>18<\/em>, 7991-7996.   &nbsp;     <\/li>\n\n\n\n<li> <em>Regioselective   Copper-catalyzed Alkylation of [2.2.2]-Acylnitroso Cycloadducts: Remarkable   Effect of the Halide of Grignard Reagents<\/em>   S. Crotti, F. Bertolini, V. Di Bussolo, M. Pineschi   <em>Org. Lett.<\/em> <strong>2010<\/strong>,   <em>12<\/em>, 1828-1830.   &nbsp;      <\/li>\n\n\n\n<li><em>Copper-Promoted   Rearrangement of 1,3-Cyclohexadiene-Acylnitroso Cycloadducts<\/em>   S.&nbsp; Crotti, F. Bertolini, F. Macchia, M.   Pineschi   <em>Tetrahedron<\/em> <em>Lett.   <\/em><strong>2010<\/strong>, <em>51<\/em>, 2284-2286.   &nbsp;     <\/li>\n\n\n\n<li> <em>Aminolysis of   Glycal-Derived Allyl Epoxides and Activated Aziridines. Effects of the   Absence of Coordination Processes on the Regio- and Stereoselectivity<\/em>   V. Di Bussolo, L. Checchia, M. R. Romano, L. Favero, M. Pineschi, P.   Crotti   <em>Tetrahedron<\/em> <strong>2010<\/strong>, <em>66<\/em>, 689-697.   &nbsp;   <\/li>\n\n\n\n<li> <em>Recent   Progress in the Synthesis of 2,3-dihydrobenzufurans<\/em>   F. Bertolini, M. Pineschi   <em>Org. Prep. Proc. Int<\/em>. <strong>2009<\/strong>,   41(5), 385-418. <\/li>\n\n\n\n<li>  &nbsp;<em>Nickel-Catalyzed   Borylative Ring-Opening of Vinyl Epoxides and Aziridines<\/em>   S. Crotti, F. Bertolini, F. Macchia, M. Pineschi   <em>Org. Lett.<\/em> <strong>2009<\/strong>, 11,   3762-3765.   &nbsp;      <\/li>\n\n\n\n<li><em>A Practical   Regioselective Ring Opening of Activated Aziridines with Organoalanes<\/em>   F. Bertolini, S. Woodward, S. Crotti, M. Pineschi   <em>Tetrahedron Lett.<\/em> <strong>2009<\/strong>, <em>50<\/em>, 4515-4518.   &nbsp;      <\/li>\n\n\n\n<li><em>Regio- and Stereoselective   Ring Opening of Allylic Epoxides<\/em>   M. Pineschi, F. Bertolini, V. Di Bussolo, P. Crotti   <em>Curr. Org. Synth<\/em>. <strong>2009<\/strong>, <em>6<\/em>(3), 290-324.   &nbsp;      <\/li>\n\n\n\n<li><em>Sequential   Copper-Catalyzed Rearrangement-Allylic Substitution of Bicyclic Hydrazines   with Grignard Reagents<\/em>   S.   Crotti, F. Bertolini, F. Macchia, M. Pineschi   <em>Adv. Synth. Catal.<\/em> <strong>2009<\/strong>, <em>351,<\/em> 869-873.   &nbsp;      <\/li>\n\n\n\n<li><em>Regio- and   Stereoselective Ring Opening of Enantiomerically Enriched 2-Aryl Oxetanes and   2-Aryl Azetidines with Aryl Borates<\/em>   F.   Bertolini, S. Crotti, V. Di Bussolo, F. Macchia, M. Pineschi   <em>J. Org. Chem.<\/em> <strong>2008<\/strong>, <em>73<\/em>, 8998-9007.   &nbsp;     <\/li>\n\n\n\n<li> <em>Synthesis of   diastereoisomeric 6-deoxy-D-allal- and 6-deoxy-D-galactal-derived allyl   epoxides and examination of the regio- and stereoselectivity in nucleophilic   addition reaction. Comparison with the corresponding 6-O-functionalized allyl   epoxides<\/em>   V.   Di Bussolo, L. Favero, M. R. Romano, M. Pineschi, P. Crotti   <em>Tetrahedron<\/em> <strong>2008<\/strong>,   <em>64<\/em>, 8188.   &nbsp;      <\/li>\n\n\n\n<li><em>Stereoselective Synthesis   of 2,3-Unsaturated-1,6-oligosaccharides by Means of a Glycal-Derived Allyl Epoxide   and N-Nosyl Aziridine<\/em>   V.   Di Bussolo, L. Checchia, M. R. Romano, M. Pineschi, P. Crotti   <em>Org. Lett.<\/em> <strong>2008<\/strong>, 10,   2493-2496.         <\/li>\n\n\n\n<li><em>Rhodium-Catalyzed   Enantioselective Desymmetrization of Bicyclic Hydrazines with Alkynylboronic   Esters <\/em>   S. Crotti, F. Bertolini, F. Macchia, M. Pineschi   <em>Chem. Comm<\/em>. <strong>2008<\/strong>, 3127.   &nbsp;      <\/li>\n\n\n\n<li><em>Mild and Stereoselective   Friedel-Crafts Alkylation of Phenol Derivatives with Vinyloxiranes: a New   Access to Cycloalkenobenzofurans<\/em>   F.   Bertolini, V. Di Bussolo, P. Crotti, M. Pineschi   <em>Synlett <\/em><strong>2007<\/strong>, 3011.   &nbsp;      <\/li>\n\n\n\n<li><em>Stereoselective   synthesis of 2,3-unsaturated-aza-O-glycosides via new diastereoisomeric   N-Cbz-imino glycal-derived allyl epoxides<\/em>   V. Di Bussolo, A. Fiasella, M. R. Romano, L. Favero, M. Pineschi, P.   Crotti   <em>Org. Lett.<\/em> <strong>2007<\/strong>, 9, 4479.         <\/li>\n\n\n\n<li><em>Synthesis and   Cyclodehydration of Hydroxyphenols: A New Stereoselective Approach to   3-Aryl-2,3-dihydrobenzofuranes <\/em>   F.   Bertolini, P. Crotti, V. Di Bussolo, F. Macchia and M. Pineschi   <em>J. Org. Chem. <\/em><strong>2007<\/strong>, <em>72<\/em>,   7761.   &nbsp;      <\/li>\n\n\n\n<li><em>Nosyl as a   stereoselectivity-improving and easily removable group in the O-glycosylation   of D-allal and D-galactal-derived allyl aziridines. Stereospecific synthesis   of 4-amino-2,3-unsaturated-O-glycosides<\/em>   V.   Di Bussolo, M. R. Romano, M. Pineschi, P. Crotti   <em>Tetrahedron<\/em> <strong>2007<\/strong>,   <em>63<\/em>, 2482.   &nbsp;      <\/li>\n\n\n\n<li><em>Rhodium-Catalyzed   Asymmetric Arylative Ring Opening of Bicyclic Hydrazines<\/em>   F.   Bertolini, F. Macchia, M. Pineschi   <em>Tetrahedron Lett. <\/em><strong>2006<\/strong>, <em>47<\/em>,   9173-9176.   &nbsp;     <\/li>\n\n\n\n<li> <em>Asymmetric Ring Opening   of Epoxides and Aziridines with Carbon Nucleophiles<\/em>   M.   Pineschi   <em>Eur. J. Org. Chem<\/em>. <strong>2006<\/strong>, 4979-4988.   &nbsp;      <\/li>\n\n\n\n<li><em>Facile Regio- and   Stereoselective Carbon-Carbon Coupling of Phenol Derivatives with Aryl   Aziridines<\/em>   F.   Bertolini, P. Crotti, F. Macchia, M. Pineschi   <em>Org. Lett<\/em>. <strong>2006<\/strong>,   <em>8<\/em>, 2627-2630.   &nbsp;      <\/li>\n\n\n\n<li><em>Catalytic Asymmetric Ring   Opening of Cyclopentadiene Heteronucleophiles Cycloadducts with   Organometallic Reagents<\/em>   F.   Del Moro, P. Crotti, F. Macchia, M. Pineschi   <em>Pure Appl. Chem.<\/em> <strong>2006<\/strong>, <em>78<\/em>, 463-467.   &nbsp;      <\/li>\n\n\n\n<li><em>Highly enantioselective   copper-phosphoramidite-catalyzed conjugate addition of dialkylzinc reagents   to acyclic a,b-unsaturated imides<\/em>   M.   Pineschi, F. Del Moro, V. Di Bussolo, F. Macchia   <em>Adv. Synth. Catal.<\/em> <strong>2006<\/strong>, <em>348,<\/em> 301.   &nbsp;      <\/li>\n\n\n\n<li><em>Stereoselective   uncatalyzed Synthesis of 2,3-unsaturated-4-N-substituted-b-O-glycosides by means of   a new D-galactal derived N-(mesyl)-aziridine<\/em>   V.   Di Bussolo, M. R. Romano, L. Favero, M. Pineschi, P. Crotti   <em>J. Org. Chem. <\/em><strong>2006<\/strong>, <em>71<\/em>,   1696.   &nbsp;     <\/li>\n\n\n\n<li> <em>A new regio- and   stereoselective intermolecular Friedel-Crafts alkylation of phenolic   substrates with aryl epoxides <\/em>   F.   Bertolini, P. Crotti, F. Macchia, M. Pineschi   <em>Tetrahedron Lett. <\/em><strong>2006<\/strong>, <em>47<\/em>,   61-64.   &nbsp;      <\/li>\n\n\n\n<li><em>Catalytic asymmetric ring   opening of 2,3-substituted norbornenes with organometallic Reagents: a new   formal aza-functionalization of cyclopentadiene <\/em>   M.   Pineschi, F. Del Moro, P. Crotti, F. Macchia   <em>Org. Lett<\/em>. <strong>2005<\/strong>,   <em>7<\/em>, 3605-3607.   &nbsp;      <\/li>\n\n\n\n<li><em>Methanolysis of   1-aryl-1,2-epoxycyclohexanes in the condensed and in the gas phase: importance   of the substituent for the reaction mechanism<\/em>   P.   Crotti, V. Di Bussolo, F. Macchia, L. Favero, M. Pineschi, L. Lucarelli, G.   Roselli, G. Renzi   <em>J. Phys. Org. Chem.<\/em> <strong>2005<\/strong>, <em>18<\/em>, 321.&nbsp;    &nbsp;      <\/li>\n\n\n\n<li><em>Stereoselective Synthesis of   4-(N-Mesylamino)-2.3-unsaturated- a-O-glycosides via a New Glycal-Derived Vinyl a-N-(Mesyl)-aziridine <\/em>   V. Di Bussolo, M. R. Romano, M. Pineschi, P. Crotti   <em>Org. Lett<\/em>. <strong>2005<\/strong>, <em>7<\/em>, 1299-1302.   &nbsp;      <\/li>\n\n\n\n<li><em>Mild metal-free syn-stereoselective ring opening of   activated epoxides and aziridines with aryl borates.<\/em>   M. Pineschi, F. Bertolini, R. M. Haak, P. Crotti, F.   Macchia   &nbsp;<em>Chem.   Commun<\/em>. <strong>2005<\/strong>, 1426-1428.   &nbsp;      <\/li>\n\n\n\n<li><em>Copper-Catalyzed Highly   Enantioselective Synthesis of Cyclic Allylic and Homoallylic Alcohols with   Dialkylzinc Reagents. <\/em>   M.   Pineschi, F. Del Moro, P. Crotti,&nbsp;V. Di Bussolo, F. Macchia   <em>Synthesis<\/em> <strong>2005<\/strong>,   334.   &nbsp;   <\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-8","page","type-page","status-publish","hentry"],"acf":[],"featured_image_src":null,"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.8 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Pubblicazioni - MAURO PINESCHI<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/people.unipi.it\/mauro_pineschi\/pubblicazioni\/\" \/>\n<meta property=\"og:locale\" content=\"it_IT\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Pubblicazioni - MAURO PINESCHI\" \/>\n<meta property=\"og:url\" content=\"https:\/\/people.unipi.it\/mauro_pineschi\/pubblicazioni\/\" \/>\n<meta property=\"og:site_name\" content=\"MAURO PINESCHI\" \/>\n<meta property=\"article:modified_time\" content=\"2025-12-23T17:26:47+00:00\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Tempo di lettura stimato\" \/>\n\t<meta name=\"twitter:data1\" content=\"10 minuti\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/people.unipi.it\\\/mauro_pineschi\\\/pubblicazioni\\\/\",\"url\":\"https:\\\/\\\/people.unipi.it\\\/mauro_pineschi\\\/pubblicazioni\\\/\",\"name\":\"Pubblicazioni - 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