Publications
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
Synlett 2019, 30 (10), 1178-1182
DOI: 10.1055/s-0037-1611737
ACS Omega 2019, 4 (2), 2669−2675
DOI: 10.1021/acsomega.8b02388
Chemistry 2019, 25 (28), 6928-6940
DOI: 10.1002/chem.201900440
Angew. Chem. Int. Ed. 2019, 58 (8), 2454-2458
DOI: 10.1002/anie.201814524
Nature 2019, 566 (7743), 224-229
DOI: 10.1038/s41586-019-0917-9
Eur. J. Org. Chem. 2019, (18), 2884-2898
DOI: 10.1002/ejoc.201900032
Molecules 2019, 24 (3), 572
DOI: 10.3390/molecules24030572
Drug Discovery Today 2019, 24 (2), 390-402
DOI: 10.1016/j.drudis.2018.10.016
New J. Chem. 2019, 43 (33), 13112-13121
DOI: 10.1039/c9nj01390c
Chem. Eur. J. 2019, 25 (24), 6053-6063
DOI: 10.1002/chem.201804953
Amino Acids 2019, 51 (2), 255-261
DOI: 10.1007/s00726-018-2660-1
J. Org. Chem. 2019, 84 (3), 1363-1371
DOI: 10.1021/acs.joc.8b02822
J. Med. Chem. 2018, 61 (23), 10793-10813
DOI: 10.1021/acs.jmedchem.8b01428
MolBank 2018, 4, 1022
DOI: 10.3390/M1022
New J. Chem. 2018, 42 (16), 13461-13470
DOI: 10.1039/c8nj02631a
New J. Chem. 2018, 42 (21), 17499-17512
DOI: 10.1039/C8NJ03460E
Biopolym. Cell. 2018, 34 (1), 59-71
DOI: 10.7124/bc.000971
J. Org. Chem. 2018, 83 (12), 6275-6289
DOI: 10.1021/acs.joc.8b00077
Org. Biomol. Chem. 2018, 16 (44), 8559-8564
DOI: 10.1039/C8OB02428F
Heterocycl. Commun. 2018, 24 (4), 177-181
DOI: 10.1515/hc-2017-0143
Tetrahedron Lett. 2018, 59 (52), 4611-4615
DOI: 10.1016/j.tetlet.2018.11.047
Eur. J. Org. Chem. 2018, 46, 6519-6523
DOI: 10.1002/ejoc.201801204
Eur. J. Org. Chem. 2018, 40, 5585-5595
DOI: 10.1002/ejoc.201800753
Org. Biomol. Chem. 2018, 16 (47), 9152-9164
DOI: 10.1039/C8OB02257G
Eur. J. Org. Chem. 2018, 47, 6682-6692
DOI: 10.1002/ejoc.201801270
Synthesis 2019, 51 (4), 848-858
DOI: 10.1055/s-0037-1611277
Angew. Chem. 2018, 57 (50), 16442-16446
DOI: 10.1002/anie.201810460
ACS Comb. Sci. 2018, 20 (11), 672-680
DOI: 10.1021/acscombsci.8b00130