Publications
Synthesis 2021, 53 (12), 2133-2141
DOI: 10.1055/a-1360-9852
Eur. J. Org. Chem. 2021, 2021 (1), 87-95
DOI: 10.1002/ejoc.202001345
Synth. Commun. 2021, 51 (6), 964-970
DOI: 10.1080/00397911.2020.1867868
J. Sulphur Chem. 2021, 42 (3), 264-280
DOI: 10.1080/17415993.2020.1855431
Chem. Heterocycl. Compd. 2020, 56 (12), 1554-1559
DOI: 10.1007/s10593-020-02849-4
Chem. Rev. 2021, 121 (3), 1670–1715
DOI: 10.1021/acs.chemrev.0c01015
J. Chem. Inf. Model. 2021, 61 (1), 179-188
DOI: 10.1021/acs.jcim.0c00936
J. Extracell. Vesicles 2020, 10 (2), e12039
DOI: 10.1002/jev2.12039
Chem. Heterocycl. Compd. 2020, 56 (11), 1411-1413
DOI: 10.1007/s10593-020-02829-8
Arch. Pharm. 2021, 354 (4), e2000275
DOI: 10.1002/ardp.202000275
Chem. Heterocycl. Compd. 2020, 56 (11), 1408-1410
DOI: 10.1007/s10593-020-02828-9
Theor. Exp. Chem. 2020, 56 (5), 283-308
DOI: 10.1007/s11237-020-09660-4
J. Org. Chem. 2021, 86 (3), 2200-2209
DOI: 10.1021/acs.joc.0c02355
ChemistrySelect 2020, 5 (43), 13569-13574
DOI: 10.1002/slct.202003500
Chem. Heterocycl. Compd. 2020, 56 (10), 1329-1334
DOI: 10.1007/s10593-020-02818-x
Eur. J. Org. Chem. 2021, 2021 (47), 6524-6529
DOI: 10.1002/ejoc.202001104
Scientific Data 2020, 7 (1), 384
DOI: 10.1038/s41597-020-00727-4
Cells 2020, 9 (10), 2272
DOI: 10.3390/cells9102272
Theor. Exp. Chem. 2020, 56 (4), 261-267
DOI: 110.1007/s11237-020-09657-z
Chem. Heterocycl. Compd. 2020, 56 (8), 1048‑1053
DOI: 10.1007/s10593-020-02771-9
Beilstein J. Org. Chem. 2020, 16, 2304-2313
DOI: 10.3762/bjoc.16.191
Chem. Rev. 2020, 120 (22), 12718-12755
DOI: 10.1021/acs.chemrev.0c00406
Org. Process Res. Dev. 2020, 24 (11), 2619‑2632
DOI: 10.1021/acs.oprd.0c00300
Org. Biomol. Chem. 2020, 18 (28), 5359-5369
DOI: 10.1039/d0ob00831a
Chem. Heterocycl. Compd. 2020, 56 (6), 719-721
DOI: 10.1007/s10593-020-02721-5
Angew. Chem. Int. Ed. 2020, 59 (46), 20515‑20521
DOI: 10.1002/anie.202004183
J. Cell. Biochem. 2020, 121 (12), 4922-4930
DOI: 10.1002/jcb.29820
Angew. Chem. Int. Ed. 2020, 59 (41), 18016‑18022
DOI: 10.1002/anie.202007651
J. Heterocycl. Chem. 2020, 57(8), 3202‑3212
DOI: 10.1002/jhet.4028
Z. Anorg. Allg. Chem. 2020, 646 (20), 1710‑1714
DOI: 10.1002/zaac.201900319
J. Biomol. NMR 2020, 74 (10-11), 555–563
DOI: 10.1007/s10858-020-00327-9
Advanced Synthesis and Catalysis 2020, 362 (15), 3229-3242
DOI: 10.1002/adsc.202000450
Bioorg. Chem. 2020, 99, 103830
DOI: 10.1016/j.bioorg.2020.103830
ChemistrySelect 2020, 5 (19), 5573-5576
DOI: 10.1002/slct.202001243
ACS Omega 2020, 5 (33), 20932-20942
DOI: 10.1021/acsomega.0c02394
J. Org. Chem. 2020, 85 (19), 12692-12702
DOI: 10.1021/acs.joc.0c01848
Chem. Heterocycl. Compd. 2020, 56 (3), 377–385
DOI: 10.1007/s10593-020-02670-z
Eur. J. Org. Chem. 2020, 2020 (22), 3261-3269
DOI: 10.1002/ejoc.202000314
Chem. Heterocycl. Compd. 2020, 56 (3), 320-325
DOI: 10.1007/s10593-020-02662-z
Chem. Heterocycl. Compd. 2020, 56 (3), 347-354
DOI: 10.1007/s10593-020-02666-9
J. Fluorine Chem. 2020, 233
DOI: 10.1016/j.jfluchem.2020.109509
J. Mol. Struct. 2020, 1210
DOI: 10.1016/j.molstruc.2020.128025
Chem. Heterocycl. Compd. 2020, 56 (3), 386–391
DOI: 10.1007/s10593-020-02671-y
Eur. J. Org. Chem. 2020, (15), 2217-2224
DOI: 10.1002/ejoc.202000346
J. Org. Chem. 2020, 85 (9), 5927-5940
DOI: 10.1021/acs.joc.0c00265
Stem Cell Rev. 2020, 16 (2), 239-250
DOI: 10.1007/s12015-020-09955-y
Eur. J. Org. Chem. 2020, (15), 2210-2216
DOI: 10.1002/ejoc.202000303
Tetrahedron Lett. 2020, 61 (12)
DOI: 10.1016/j.tetlet.2020.151645
Synthesis 2020, 52 (13), 1915-1926
DOI: 10.1055/s-0039-1707987
Twisting and Turning the Sulfonamide Bond: A Synthetic, Quantum Chemical, and Crystallographic Study
J. Org. Chem. 2020, 85 (8), 5288-5299
DOI: 10.1021/acs.joc.9b03394