Publications
![An Approach to 3-Oxa-7-azabicyclo[3.3.0]octanes – Bicyclic Morpholine Surrogates](/images/publications/s-0036-1588785.png)
Synthesis 2017, 49 (14), 3112-3117
DOI: 10.1055/s-0036-1588785
Angew. Chem. 2017, 129 (30), 8865–8869
DOI: 10.1002/ange.201703801

Biochim. Biophys. Acta 2017, 1859 (10), 1828‑1837
DOI: 10.1016/j.bbamem.2017.06.003
Monatsh. Chem. 2017, 148 (6), 1035-1041
DOI: 10.1007/s00706-016-1905-5

Molecules 2017, 22 (5), 804
DOI: 10.3390/molecules22050804
Tetrahedron Lett. 2017, 58 (18), 1751-1754
DOI: 10.1016/j.tetlet.2017.03.062
Monatsh. Chem. 2017, 148 (5), 939-946
DOI: 10.1007/s00706-016-1884-6

Mol. Diver. 2017, 21 (2), 427-436
DOI: 10.1007/s11030-017-9737-8
J. Fluorine Chem. 2017, 196, 88-97
DOI: 10.1016/j.jfluchem.2016.09.014
Chem. Heterocycl. Compd. 2017, 53 (4), 484‑490
DOI: 10.1007/s10593-017-2078-9
Biophys. J. 2017, 112 (4), 630-642
DOI: 10.1016/j.bpj.2016.12.040

Eur. J. Med. Chem. 2017, 127, 357-368
DOI: 10.1016/j.ejmech.2017.01.005

Tetrahedron 2017, 73 (6), 750‑757
DOI: 10.1016/j.tet.2016.12.052

RSC Adv. 2016, 6 (27), 22737-22748
DOI: 10.1039/C6RA01548D

Tetrahedron Lett. 2016, 57 (12), 1382-1384
DOI: 10.1016/j.tetlet.2016.02.069

ACS Comb. Sci. 2016, 18 (10), 616-624
DOI: 10.1021/acscombsci.6b00103
Russ. J. Org. Chem. 2016, 52 (5), 661-669
DOI: 10.1134/s1070428016050080

Mol. Diver. 2016, 20 (1), 1-7
DOI: 10.1007/s11030-015-9633-z

Tetrahedron Lett. 2016, 57 (17), 1909-1911
DOI: 10.1016/j.tetlet.2016.03.066

RSC Adv. 2016, 6 (96), 93707-93714
DOI: 10.1039/C6RA09353A

Biochim. Biophys. Acta 2016, 1858 (9), 2019‑2027
DOI: 10.1016/j.bbamem.2016.06.002

Eur. J. Org. Chem. 2016, 33, 5485-5493
DOI: 10.1002/ejoc.201600947

Tetrahedron Lett. 2016, 57 (9), 1056-1059
DOI: 10.1016/j.tetlet.2016.01.094

Tetrahedron 2016, 72 (10), 1351-1356
DOI: 10.1016/j.tet.2016.01.032

Angew. Chem. Int. Ed. 2016, 55 (47), 1459514599
DOI: 10.1002/anie.201607161
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