Publications
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
Chem. Heterocycl. Compd. 2019, 55 (4-5), 379-385
DOI: 10.1007/s10593-019-02468-8
An approach to the synthesis of 3-substituted piperidines bearing partially fluorinated alkyl groups
J. Fluorine Chem. 2019, 224, 61-66
DOI: 10.1016/j.jfluchem.2019.05.006
Eur. J. Org. Chem. 2019, (23), 3744-3750
DOI: 10.1002/ejoc.201900485
Eur. J. Org. Chem. 2019 (22), 3636-3648
DOI: 10.1002/ejoc.201900450
Beilstein J. Org. Chem. 2019, 15, 1032-1045
DOI: 10.3762/bjoc.15.101
ChemistrySelect 2019, 4 (17), 4933-4937
DOI: 10.1002/slct.201900650
Org. Biomol. Chem. 2019, 17, 4342-4349
DOI: 10.1039/c9ob00393b
ACS Omega 2019, 4 (4), 7498-7515
DOI: 10.1021/acsomega.9b00896
Chem. Heterocycl. Compd. 2019, 55 (3), 196‑198
DOI: 10.1007/s10593-019-02440-6
J. Org. Chem. 2019, 84 (13), 8487-8496
DOI: 10.1021/acs.joc.9b00719
J. Am. Chem. Soc. 2019, 141 (16), 6726-6739
DOI: 10.1021/jacs.9b02238
Eur. J. Org. Chem. 2019, (27), 4311-4319
DOI: 10.1002/ejoc.201900123
Molecules 2019, 24 (7), 1249-1260
DOI: 10.3390/molecules24071249
J. Heterocycl. Chem. 2019, 56 (5), 1605-1612
DOI: 10.1002/jhet.3541
Chem. Heterocycl. Compd. 2019, 55 (2), 184‑188
DOI: 10.1007/s10593-019-02437-1
Chem. Heterocycl. Compd. 2019, 55 (2), 189‑192
DOI: 10.1007/s10593-019-02438-0
J. Fluorine Chem. 2019, 217, 80-89
DOI: 10.1016/j.jfluchem.2018.11.006
Chem. Heterocycl. Compd. 2019, 55 (3), 202‑204
DOI: 10.1007/s10593-019-02442-4
Regen. Med. 2019, 14 (3), 243-255
DOI: 10.2217/rme-2019-0001
Org. Lett. 2019, 21 (7), 2340-2345
DOI: 10.1021/acs.orglett.9b00622
Org. Biomol. Chem. 2019, 17 (11), 2839-2849
DOI: 10.1039/c8ob02812e
Eur. J. Med. Chem. 2019, 165, 258-272
DOI: 10.1016/j.ejmech.2019.01.010