Publications
Curr. Comput. Aided. Drug Des. 2016, 12 (1), 29-41
DOI: 10.2174/1573409912666160126142236
J. Org. Chem. 2016, 81 (14), 5803-5813
DOI: 10.1021/acs.joc.6b00628
Tetrahedron: Asymmetry 2016, 27 (7-8), 341‑345
DOI: 10.1016/j.tetasy.2016.02.012
J. Enzyme Inhib. Med. Chem. 2016, 31 (6), 1707-1711
DOI: 10.3109/14756366.2016.1156676
Biorg. Med. Chem. 2016, 24 (13), 2954-2963
DOI: 10.1016/j.bmc.2016.04.065
J. Enzyme Inhib. Med. Chem. 2016, 31 (6), 1404-1410
DOI: 10.3109/14756366.2016.1142984
Biorg. Med. Chem. 2016, 24 (21), 5481-5494
DOI: 10.1016/j.bmc.2016.09.004
J. Enzyme Inhib. Med. Chem. 2016, 1-8, 29-36
DOI: 10.1080/14756366.2016.1230110
Angew. Chem. Int. Ed. 2016, 55 (47), 1478814792
DOI: 10.1002/anie.201608116
Asian J. Org. Chem. 2016, 5 (4), 513-520
DOI: 10.1002/ajoc.201500519
Russ. J. Org. Chem. 2016, 52 (4), 607-609
DOI: 10.1134/s107042801604028x
Practical Synthesis of Fluorinated Piperidine Analogues Based on the 2-Azaspiro[3.3]heptane Scaffold
Synlett 2016, 27 (12), 1824-1827
DOI: 10.1055/s-0035-1562113
Eur. J. Org. Chem. 2016, 28, 4782-4786
DOI: 10.1002/ejoc.201600953
Tetrahedron 2016, 72 (7), 1036-1041
DOI: 10.1016/j.tet.2015.12.081
RSC Adv. 2016, 6 (31), 25713-25723
DOI: 10.1039/C6RA02365G
Eur. J. Org. Chem. 2016, 12, 2120-2130
DOI: 10.1002/ejoc.201501579
Angew. Chem. Int. Ed. 2016, 55 (18), 5493‑5496
DOI: 10.1002/anie.201600506
Org. Lett. 2016, 18 (14), 3406-3409
DOI: 10.1021/acs.orglett.6b01565
Helv. Chim. Acta 2016, 99 (8), 621-631
DOI: 10.1002/hlca.201600062
Synth. Commun. 2016, 46 (6), 551-555
DOI: 10.1080/00397911.2016.1156131
Bioorg. Med. Chem. Lett. 2015, 25 (16), 3105‑3111
DOI: 10.1016/j.bmcl.2015.06.018
Synthesis 2015, 47 (24), 3963-3971
DOI: 10.1055/s-0035-1560199
Tetrahedron: Asymmetry 2015, 26 (2122), 1268-1272
DOI: 10.1016/j.tetasy.2015.09.015
J. Fluorine Chem. 2015, 171 174-176
DOI: 10.1016/j.jfluchem.2014.06.003
Inorg. Chem. 2015, 54 (11), 5169-5181
DOI: 10.1021/ic503061z
Tetrahedron Lett. 2015, 56 (10), 1259-1262
DOI: 10.1016/j.tetlet.2015.01.136
Scientia Pharmaceutica 2015, 83 (3), 535-548
DOI: 10.3797/scipharm.1502-01
Tetrahedron 2015, 71 (40), 7567-7574
DOI: 10.1016/j.tet.2015.08.009
Theor. Exp. Chem. 2015, 51 (2), 133-139
DOI: 10.1007/s11237-015-9408-8
RSC Adv. 2015, 5 (26), 20498-20502
DOI: 10.1039/C4RA10688A
Theor. Exp. Chem. 2015, 51 (1), 45-53
DOI: 10.1007/s11237-015-9396-8
Chem. Heterocycl. Compd. 2015, 51 (4), 310‑319
DOI: 10.1007/s10593-015-1700-y
Tetrahedron 2015, 71 (8), 1311-1321
DOI: 10.1016/j.tet.2014.12.057
Beilstein J. Org. Chem. 2015, 11 16-24
DOI: 10.3762/bjoc.11.3
Angew. Chem. Int. Ed. 2015, 54 (22), 6373‑6373
DOI: 10.1002/anie.201503577
Eur. J. Org. Chem. 2015, 33, 7235-7239
DOI: 10.1002/ejoc.201501027
Org. Biomol. Chem. 2015, 13 (11), 3438-3445
DOI: 10.1039/C4OB02670E
Angew. Chem. Int. Ed. 2015, 54 (22), 6558‑6561
DOI: 10.1002/anie.201501529
J. Fluorine Chem. 2015, 175 73-83
DOI: 10.1016/j.jfluchem.2015.03.008
Org. Biomol. Chem. 2015, 13 (11), 3171-3181
DOI: 10.1039/C5OB00034C
Eur. J. Org. Chem. 2015, 11, 2482-2491
DOI: 10.1002/ejoc.201500032
J. Org. Chem. 2015, 80 (24), 12258-11264
DOI: 10.1021/acs.joc.5b02171
J. Am. Chem. Soc. 2015, 137 (2), 926-930
DOI: 10.1021/ja511460a
Synthesis 2015, 26 (08), 1123-1130
DOI: 10.1055/s-0034-1380116
Synthesis 2015, 47 (03), 367-367
DOI: 10.1055/s-0034-1379456
Eur. J. Org. Chem. 2015, 4, 886-891
DOI: 10.1002/ejoc.201403295
Org. Lett. 2015, 17 (8), 1922-1925
DOI: 10.1021/acs.orglett.5b00608
Chem. Heterocycl. Compd. 2015, 51 (4), 389‑392
DOI: 10.1007/s10593-015-1713-6
J. Org. Chem. 2015, 80 (8), 3974-3981
DOI: 10.1021/acs.joc.5b00323
Eur. J. Org. Chem. 2015, 29, 6466-6471
DOI: 10.1002/ejoc.201500746