Publications
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
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
Chem. Heterocycl. Compd. 2020, 56 (2), 213–218
DOI: 10.1007/s10593-020-02646-z
Nature 2020, 580 (7805), 663-668
DOI: 10.1038/s41586-020-2117-z
Eur. J. Org. Chem. 2020, 2020 (9), 1069-1077
DOI: 10.1002/ejoc.201901833
Chem. Heterocycl. Compd. 2020, 56 (2), 170-172
DOI: 10.1007/s10593-020-02641-4
J. Fluorine Chem. 2020, 231, 109461
DOI: 10.1016/j.jfluchem.2020.109461
Angew. Chem. 2020, 59 (18), 7161-7167
DOI: 10.1002/anie.202000548
Nature 2020, 579 (7800), 609-614
DOI: 10.1038/s41586-020-2027-0
Eur. J. Org. Chem. 2020, 2020 (23), 3367-3377
DOI: 10.1002/ejoc.202000078
Chem. Heterocycl. Compd. 2020, 56 (1), 39-41
DOI: 10.1007/s10593-020-02619-2
Synlett 2020, 31 (06), 565-574
DOI: 10.1055/s-0037-1610744
J. Org. Chem. 2020, 85 (5), 3110-3124
DOI: 10.1021/acs.joc.9b03011
Chem. Eur. J. 2020, 26 (6), 1196-1237
DOI: 10.1002/chem.201903232
J. Fluorine Chem. 2020, 229
DOI: 10.1016/j.jfluchem.2019.109407
Chem. Eur. J. 2020, 26 (1), 89-101
DOI: 10.1002/chem.201903335
J. Enzyme Inhib. Med. Chem. 2020, 35 (1), 306‑310
DOI: 10.1080/14756366.2019.1698562
J. Enzyme Inhib. Med. Chem. 2020, 35 (1), 165‑171
DOI: 10.1080/14756366.2019.1693556
J. Heterocycl. Chem. 2020, 57 (1), 317-326
DOI: 10.1002/jhet.3779
J. Org. Chem. 2020, 85 (4), 2321-2337
DOI: 10.1021/acs.joc.9b03044
Sci. Rep. 2019, 9 (1), 19585
DOI: 10.1038/s41598-019-55069-y
J. Org. Chem. 2019, 84 (24), 15877-15899
DOI: 10.1021/acs.joc.9b02264
Sci. Rep. 2019, 9 (1), 17938
DOI: 10.1038/s41598-019-54212-z
Chem. Heterocycl. Compd. 2019, 55 (11), 1007–1012
DOI: 10.1007/s10593-019-02570-x
Chem. Heterocycl. Compd. 2019, 55 (11), 1070-1074
DOI: 10.1007/s10593-019-02579-2
Chem. Heterocycl. Compd. 2019, 55 (11), 1092‑1097
DOI: 10.1007/s10593-019-02583-6
Chem. Heterocycl. Compd. 2019, 55 (11), 1065-1069
DOI: 10.1007/s10593-019-02578-3
J. Org. Chem. 2019, 84 (21), 13908-13921
DOI: 10.1021/acs.joc.9b02067
J. Org. Chem. 2019, 84 (23), 15212-15225
DOI: 10.1021/acs.joc.9b02258
Chem. Heterocycl. Compd. 2019, 55 (9), 893‑896
DOI: 10.1007/s10593-019-02554-x
Chem. Heterocycl. Compd. 2019, 55 (10), 933‑935
DOI: 10.1007/s10593-019-02558-7
Adv. Synth. Catal. 2019, 361 (23), 5428-5439
DOI: 10.1002/adsc.201900879
Org. Lett. 2019, 21 (22), 8909-8914
DOI: 10.1021/acs.orglett.9b03080
J. Org. Chem. 2019, 84 (23), 15106-15117
DOI: 10.1021/acs.joc.9b01947
Tetrahedron Lett. 2019, 60 (39), 151089 - 4
DOI: 10.1016/j.tetlet.2019.151089