– publications –
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Spiro Compounds: Synthesis and Applications; John Wiley & Sons, Inc. 2022, 35-64 | DOI: 10.1002/9781119567646.ch3; ISBN: 9781119567646
44 |
J. Org. Chem. 2021, 86, 4326-4335 | DOI: 10.1021/acs.joc.0c02998
43 |
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CO2 as building block in organic synthesis; Wiley-VCH Verlag GmbH & Co. 2020, 225-252 | DOI: 10.1002/9783527821952.ch7 ; ISBN: 9783527821952
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38 |
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Beilstein J. Org. Chem. 2018, 14, 2418-2424 | DOI: 10.3762/bjoc.14.219 – invited contribution to “Photoredox catalysis for novel organic reactions” thematic issue –
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33 |
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ChemSusChem 2018, 11, 3056-3070 | DOI: 10.1002/cssc.201801063 – amongst the top 10% most downloaded ChemSusChem articles in 2018-2019 –
31 |
J. Am. Chem. Soc. 2017, 139, 8432-8435 | DOI: 10.1021/jacs.7b05045 – featured in the 2018 JACS Young Investigator Virtual Issue –
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Chem. Commun. 2016, 52, 6821-6824 | DOI: 10.1039/C6CC01026A
29 |
Tetrahedron 2014, 70, 75-83 | DOI: 10.1016/j.tet.2013.11.028
28 |
27 |
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Chem. Commun. 2013, 1184-1186 | DOI: 10.1039/C2CC38659C – highlighted in Synfacts 2013, 9, 0355 | DOI: 10.1055/s-0032-1318212 –
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Stereoselective organocatalysis: bond formation methodologies and activation modes; Wiley 2013, 351-380 | ISBN: 978-1-118-60470-0
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Stereoselective organocatalysis: bond formation methodologies and activation modes; Wiley 2013, 1-10 | ISBN: 978-1-118-60470-0
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Eur. J. Org. Chem. 2013, 5262-5265 | DOI: 10.1002/ejoc.201300899
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Studies in Natural Products Chemistry (Bioactive Natural Products); Elsevier Science Publishers 2013, 71-132 | ISBN: 978-0-444-596031
21 |
Tetrahedron Lett. 2012, 53, 4124-412 | DOI: 10.1016/j.tetlet.2012.05.121
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Org. Biomol. Chem. 2012, 10, 431-439 | DOI: 10.1039/C1OB06503C
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Chem. Eur. J. 2011, 17, 2018-2037 | DOI: 10.1002/chem.201001546 – amongst the top 20 most cited papers in Chemistry-A European Journal in 20th anniversary of the journal (1995-2015) –
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Org. Biomol. Chem. 2011, 9, 7986-7989 | DOI: 10.1039/C1OB06308A
17 |
Chem. Commun. 2010, 46, 6953-6955 | DOI: 10.1039/c0cc01522a
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Chem. Eur. J. 2010, 16, 5354-5361 | DOI: 10.1002/chem.200903025
15 |
Chem. Eur. J. 2010, 16, 1142-1148 | DOI: 10.1002/chem.200902678
14 |
Chem. Soc. Rev. 2010, 39, 2018-2033 | DOI: 10.1039/B911852G
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New. J. Chem. 2010, 34, 1816-1820 | DOI: 10.1039/C0NJ00321B
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Synlett 2010, 13, 1833-1908 | DOI: 10.1055/s-0030-1257988
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Mini Rev Org Chem 2010, 7, 1-9 | DOI: 10.2174/1570193X11007010001
10 |
Tetrahedron Lett. 2009, 50, 6624-6626 | DOI: 10.1016/j.tetlet.2009.09.038
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Chem. Eur. J. 2009, 15, 11095-11099 | DOI: 10.1002/chem.200901806
8 |
Tetrahedron Lett. 2009, 50, 5021-5024 | DOI: 10.1016/j.tetlet.2009.06.092
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Chem. Eur. J. 2009, 15, 7035-7038 | DOI: 10.1002/chem.200900991
6 |
Chem. Eur. J. 2009, 15, 6564-6568 | DOI: 10.1002/chem.200900488
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Targets in heterocyclic chemistry; Springer 2009, 13, 147-174. Chapter 5 | ISBN: 978-88-86208-62-8
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Cur Org Chem 2009, 13, 1432-1474 | DOI: 10.2174/138527209789055054
3 |
Eur. J. Org. Chem. 2009, 3075-3080 | DOI: 10.1002/ejoc.200900209
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Lett. Org. Chem. 2009, 6, 293-296 | DOI: 10.2174/157017809788489855
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Eur. J. Org. Chem. 2009, 199-203 | DOI: 10.1002/ejoc.200801005