Publications
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
Nature 2019, 573 (7774), 398-402
DOI: 10.1038/s41586-019-1539-y
Molecules 2019, 24 (17), 3096
DOI: 10.3390/molecules24173096
Chem. Heterocycl. Compd. 2019, 55 (8), 692‑694
DOI: 10.1007/s10593-019-02521-6
Chem. Heterocycl. Compd. 2019, 55 (7), 601-603
DOI: 10.1007/s10593-019-02503-8
Eur. J. Org. Chem. 2019, (34), 5937-5949
DOI: 10.1002/ejoc.201901001
Eur. J. Org. Chem. 2019, (30), 4962-4967
DOI: 10.1002/ejoc.201900914
Eur. J. Org. Chem. 2019, (33), 5624-5635
DOI: 10.1002/ejoc.201900648
Phosphorus, Sulfur, Silicon Relat. Elem. 2019, 194 (12), 1149-1157
DOI: 10.1080/10426507.2019.1633318
ACS Omega 2019, 4 (1), 203-213
DOI: 10.1021/acsomega.8b02595
J. Sulfur Chem. 2019, 40 (6), 629-640
DOI: 10.1080/17415993.2019.1633326
Tetrahedron 2019, 75 (25), 3472-3478
DOI: 10.1016/j.tet.2019.05.005
Eur. J. Org. Chem. 2019, (22), 3553-3559
DOI: 10.1002/ejoc.201801750
Eur. J. Med. Chem. 2019, 174, 292-308
DOI: 10.1016/j.ejmech.2019.04.052
Chem. Heterocycl. Compd. 2019, 55 (4-5), 359-366
DOI: 10.1007/s10593-019-02465-x
Chem. Heterocycl. Compd. 2019, 55 (4-5), 367-373
DOI: 10.1007/s10593-019-02466-w
Chem. Heterocycl. Compd. 2019, 55 (4-5), 416-420
DOI: 10.1007/s10593-019-02474-w
Chem. Heterocycl. Compd. 2019, 55 (4-5), 421-434
DOI: 10.1007/s10593-019-02475-9