Publications

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
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