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Leonardo Degennaro
Leonardo Degennaro
Dipartimento Farmacia University of Bari
Verified email at uniba.it
Title
Cited by
Cited by
Year
Recent advances in the stereoselective synthesis of aziridines
L Degennaro, P Trinchera, R Luisi
Chemical Reviews 114 (16), 7881-7929, 2014
4382014
Transfer of electrophilic NH using convenient sources of ammonia: direct synthesis of NH sulfoximines from sulfoxides
M Zenzola, R Doran, L Degennaro, R Luisi, JA Bull
Angewandte Chemie 128 (25), 7319-7323, 2016
2042016
Contribution of microreactor technology and flow chemistry to the development of green and sustainable synthesis
F Fanelli, G Parisi, L Degennaro, R Luisi
Beilstein Journal of Organic Chemistry 13 (1), 520-542, 2017
1882017
Synthesis of NH-sulfoximines from sulfides by chemoselective one-pot N-and O-transfers
A Tota, M Zenzola, SJ Chawner, S St John-Campbell, C Carlucci, ...
Chemical communications 53 (2), 348-351, 2017
1622017
Exploiting a “beast” in carbenoid chemistry: Development of a straightforward direct nucleophilic fluoromethylation strategy
G Parisi, M Colella, S Monticelli, G Romanazzi, W Holzer, T Langer, ...
Journal of the American Chemical Society 139 (39), 13648-13651, 2017
1122017
Recent advances in the chemistry of metallated azetidines
D Antermite, L Degennaro, R Luisi
Organic & Biomolecular Chemistry 15 (1), 34-50, 2017
1112017
Titanium dioxide as a catalyst in biodiesel production
C Carlucci, L Degennaro, R Luisi
Catalysts 9 (1), 75, 2019
892019
Synthesis and Transformations of NH‐Sulfoximines
M Andresini, A Tota, L Degennaro, JA Bull, R Luisi
Chemistry–A European Journal 27 (69), 17293-17321, 2021
842021
Modular and chemoselective strategy for the direct access to α-fluoroepoxides and aziridines via the addition of fluoroiodomethyllithium to carbonyl-like compounds
S Monticelli, M Colella, V Pillari, A Tota, T Langer, W Holzer, L Degennaro, ...
Organic letters 21 (2), 584-588, 2019
682019
External trapping of halomethyllithium enabled by flow microreactors
L Degennaro, F Fanelli, A Giovine, R Luisi
Advanced Synthesis & Catalysis 357 (1), 21-27, 2015
662015
Fluoro‐substituted methyllithium chemistry: external quenching method using flow microreactors
M Colella, A Tota, Y Takahashi, R Higuma, S Ishikawa, L Degennaro, ...
Angewandte Chemie 132 (27), 11016-11020, 2020
642020
Synthesis of Sulfonimidamides from Sulfenamides via an Alkoxy‐amino‐λ6‐sulfanenitrile Intermediate
EL Briggs, A Tota, M Colella, L Degennaro, R Luisi, JA Bull
Angewandte Chemie International Edition 58 (40), 14303-14310, 2019
632019
Stereospecific β-lithiation of oxazolinyloxiranes: synthesis of α, β-epoxy-γ-butyrolactones
V Capriati, L Degennaro, R Favia, S Florio, R Luisi
Organic Letters 4 (9), 1551-1554, 2002
602002
Highly chemoselective NH-and O-transfer to thiols using hypervalent iodine reagents: synthesis of sulfonimidates and sulfonamides
A Tota, S St John-Campbell, EL Briggs, GO Estévez, M Afonso, ...
Organic letters 20 (9), 2599-2602, 2018
592018
Chiral switchable catalysts for dynamic control of enantioselectivity
G Romanazzi, L Degennaro, P Mastrorilli, R Luisi
ACS Catalysis 7 (6), 4100-4114, 2017
592017
Flow technology for organometallic-mediated synthesis
L Degennaro, C Carlucci, S De Angelis, R Luisi
Journal of Flow Chemistry 6 (3), 136-166, 2016
562016
Synthesis of 1, 2, 3, 4-tetrahydroisoquinolines by microreactor-mediated thermal isomerization of laterally lithiated arylaziridines.
A Giovine, B Musio, L Degennaro, A Falcicchio, A Nagaki, J Yoshida, ...
Chemistry (Weinheim an der Bergstrasse, Germany) 19 (6), 1872-1876, 2013
532013
A stereospecific synthesis of oxazolinyloxiranes
A Abbotto, V Capriati, L Degennaro, S Florio, R Luisi, M Pierrot, ...
The Journal of Organic Chemistry 66 (9), 3049-3058, 2001
522001
Flow microreactor technology for taming highly reactive chloroiodomethyllithium carbenoid: Direct and chemoselective synthesis of α-chloroaldehydes
P Musci, M Colella, A Sivo, G Romanazzi, R Luisi, L Degennaro
Organic letters 22 (9), 3623-3627, 2020
512020
Regioselective functionalization of 2-arylazetidines: Evaluating the ortho-directing ability of the azetidinyl ring and the α-directing ability of the N-substituent
L Degennaro, M Zenzola, P Trinchera, L Carroccia, A Giovine, ...
Chemical communications 50 (14), 1698-1700, 2014
472014
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