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21
Deprotonative Metallation of Benzofuran and Benzothiophene Derivatives for the Formation of Tetracyclic and Pentacyclic Heteroaromatic Compounds
Deprotonative Metallation of Benzofuran and Benzothiophene Derivatives for the Formation of Tetracyclic and Pentacyclic Heteroaromatic Compounds
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Deprotonative Metallation of Benzofuran and Benzothiophene Derivatives for the Formation of Tetracyclic and Pentacyclic Heteroaromatic Compounds

European journal of organic chemistry, 2024 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1434-193X ;EISSN: 1099-0690 ;DOI: 10.1002/ejoc.202400374

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22
An electrochemical access to 2-amino-2,3-dihydro-1,4-benzodioxanes derived from hydroxytyrosol
An electrochemical access to 2-amino-2,3-dihydro-1,4-benzodioxanes derived from hydroxytyrosol
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An electrochemical access to 2-amino-2,3-dihydro-1,4-benzodioxanes derived from hydroxytyrosol

Organic & biomolecular chemistry, 2024, Vol.22 (5), p.1057-1063 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1477-0520 ;EISSN: 1477-0539 ;DOI: 10.1039/d3ob01858j

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23
Mn-Mediated α-Radical Addition of Carbonyls to Olefins: Systematic Study, Scope, and Electrocatalysis
Mn-Mediated α-Radical Addition of Carbonyls to Olefins: Systematic Study, Scope, and Electrocatalysis
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Mn-Mediated α-Radical Addition of Carbonyls to Olefins: Systematic Study, Scope, and Electrocatalysis

Journal of organic chemistry, 2022-05, Vol.87 (9), p.5690-5702 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/acs.joc.2c00054

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24
Palladium catalysis: dependence of the C-C bond synthesis efficiency on carboxylate ligand and alkali metal carboxylate or carboxylic acid additive. Part A: the C(sp 2 )-C(sp 2 ), C(sp 2 )-C(sp 3 ) and C(sp 3 )-C(sp 3 ) bonds
Palladium catalysis: dependence of the C-C bond synthesis efficiency on carboxylate ligand and alkali metal carboxylate or carboxylic acid additive. Part A: the C(sp 2 )-C(sp 2 ), C(sp 2 )-C(sp 3 ) and C(sp 3 )-C(sp 3 ) bonds
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Palladium catalysis: dependence of the C-C bond synthesis efficiency on carboxylate ligand and alkali metal carboxylate or carboxylic acid additive. Part A: the C(sp 2 )-C(sp 2 ), C(sp 2 )-C(sp 3 ) and C(sp 3 )-C(sp 3 ) bonds

Advanced synthesis & catalysis, 2023-10, Vol.365 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1615-4150 ;EISSN: 1615-4169 ;DOI: 10.1002/adsc.202300903

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25
Announcement: Top reviewers for The Journal of Chemical Physics 2017
Announcement: Top reviewers for The Journal of Chemical Physics 2017
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Announcement: Top reviewers for The Journal of Chemical Physics 2017

The Journal of chemical physics, 2018-07, Vol.149 (1), p.010201 [Peer Reviewed Journal]

Author(s) ;2018 Author(s). Published by AIP Publishing. ;ISSN: 0021-9606 ;EISSN: 1089-7690 ;DOI: 10.1063/1.5043197 ;PMID: 29981560 ;CODEN: JCPSA6

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26
CO 2 Hydroboration: Impact of the Boryl Moieties on the Reactivity of Four Bis(boryl)acetal Compounds toward 2,6‐Diisopropylaniline
CO 2 Hydroboration: Impact of the Boryl Moieties on the Reactivity of Four Bis(boryl)acetal Compounds toward 2,6‐Diisopropylaniline
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CO 2 Hydroboration: Impact of the Boryl Moieties on the Reactivity of Four Bis(boryl)acetal Compounds toward 2,6‐Diisopropylaniline

European journal of organic chemistry, 2023-08, Vol.26 (30) [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1434-193X ;EISSN: 1099-0690 ;DOI: 10.1002/ejoc.202300525

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27
Remote Radical Trifluoromethylation: A Unified Approach to the Selective Synthesis of γ-Trifluoromethyl α,β-Unsaturated Carbonyl Compounds
Remote Radical Trifluoromethylation: A Unified Approach to the Selective Synthesis of γ-Trifluoromethyl α,β-Unsaturated Carbonyl Compounds
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Remote Radical Trifluoromethylation: A Unified Approach to the Selective Synthesis of γ-Trifluoromethyl α,β-Unsaturated Carbonyl Compounds

Organic letters, 2022-12, Vol.24 (51), p.9375-9380 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1523-7060 ;EISSN: 1523-7052 ;DOI: 10.1021/acs.orglett.2c03676

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28
Improved slow magnetic relaxation in optically pure helicene-based Dy(III) single molecule magnets
Improved slow magnetic relaxation in optically pure helicene-based Dy(III) single molecule magnets
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Improved slow magnetic relaxation in optically pure helicene-based Dy(III) single molecule magnets

Chemical communications (Cambridge, England), 2016, Vol.52 (100), p.14474-14477 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1359-7345 ;EISSN: 1364-548X ;DOI: 10.1039/C6CC08638A ;PMID: 27904894

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29
Tuning the Charge Transfer in lambda 5 -Phosphinines with Amino-substituents
Tuning the Charge Transfer in lambda 5 -Phosphinines with Amino-substituents
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Tuning the Charge Transfer in lambda 5 -Phosphinines with Amino-substituents

Organic letters, 2022-09, Vol.24 (37) [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1523-7060 ;EISSN: 1523-7052 ;DOI: 10.1021/acs.orglett.2c02846

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30
Recent Developments in Asymmetric Nazarov Reactions
Recent Developments in Asymmetric Nazarov Reactions
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Recent Developments in Asymmetric Nazarov Reactions

Current organic chemistry, 2024 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1385-2728 ;EISSN: 1875-5348 ;DOI: 10.2174/0113852728296619240321060646

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31
Professor Cees Veeger and the early years of bioinorganic chemistry
Professor Cees Veeger and the early years of bioinorganic chemistry
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Professor Cees Veeger and the early years of bioinorganic chemistry

The FEBS journal, 2018-05, Vol.285 (9), p.1560-1562 [Peer Reviewed Journal]

2018 Federation of European Biochemical Societies ;Copyright © 2018 Federation of European Biochemical Societies ;ISSN: 1742-464X ;EISSN: 1742-4658 ;DOI: 10.1111/febs.14470 ;PMID: 29701011

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32
Biogas reforming to syngas in a DBD plasma reactor with dielectric materials packing: Effect of H2S on the conversion of CH4 and CO2
Biogas reforming to syngas in a DBD plasma reactor with dielectric materials packing: Effect of H2S on the conversion of CH4 and CO2
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Biogas reforming to syngas in a DBD plasma reactor with dielectric materials packing: Effect of H2S on the conversion of CH4 and CO2

Biomass and Bioenergy, 2023, Vol.173, p.106781 [Peer Reviewed Journal]

ISSN: 0961-9534 ;EISSN: 1873-2909 ;DOI: 10.1016/j.biombioe.2023.106781

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33
From A 3 /KA 2 to AYA/KYA multicomponent coupling reactions with terminal ynamides as alkyne surrogates – a direct, green route to γ-amino-ynamides
From A 3 /KA 2 to AYA/KYA multicomponent coupling reactions with terminal ynamides as alkyne surrogates – a direct, green route to γ-amino-ynamides
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From A 3 /KA 2 to AYA/KYA multicomponent coupling reactions with terminal ynamides as alkyne surrogates – a direct, green route to γ-amino-ynamides

Green chemistry : an international journal and green chemistry resource : GC, 2022-08, Vol.24 (17), p.6467-6475 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1463-9262 ;EISSN: 1463-9270 ;DOI: 10.1039/D2GC00966H

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34
Iodination of terminal alkynes using KI/CuSO4 – A facile method with potential for radio-iodination
Iodination of terminal alkynes using KI/CuSO4 – A facile method with potential for radio-iodination
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Iodination of terminal alkynes using KI/CuSO4 – A facile method with potential for radio-iodination

2019 Elsevier Ltd. All rights reserved. This manuscript is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Licence http://creativecommons.org/licenses/by-nc-nd/4.0 ;ISSN: 0040-4039 ;EISSN: 1873-3581

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35
Regio- and stereocontrolled synthesis of borylated E -enynes, Z -enediynes and derivatives from alkenyl-1,2-bis-(boronates)
Regio- and stereocontrolled synthesis of borylated E -enynes, Z -enediynes and derivatives from alkenyl-1,2-bis-(boronates)
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Regio- and stereocontrolled synthesis of borylated E -enynes, Z -enediynes and derivatives from alkenyl-1,2-bis-(boronates)

Organic & biomolecular chemistry, 2023, Vol.21 (37), p.7567-7571 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1477-0520 ;EISSN: 1477-0539 ;DOI: 10.1039/d3ob00543g

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36
RETRACTED ARTICLE: An in vitro model for quantifying chemical transfer from fabric to and through skin
RETRACTED ARTICLE: An in vitro model for quantifying chemical transfer from fabric to and through skin
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RETRACTED ARTICLE: An in vitro model for quantifying chemical transfer from fabric to and through skin

Journal of exposure science & environmental epidemiology, 2019-10, Vol.29 (6), p.864-864 [Peer Reviewed Journal]

COPYRIGHT 2019 Nature Publishing Group ;COPYRIGHT 2019 Nature Publishing Group ;Copyright Nature Publishing Group Nov 2019 ;Nature America, Inc., part of Springer Nature 2018. ;ISSN: 1559-0631 ;EISSN: 1559-064X ;DOI: 10.1038/s41370-018-0047-8 ;PMID: 29855516

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37
Sonochemically‐Induced Reduction of Alkenes to Alkanes with Ammonnia
Sonochemically‐Induced Reduction of Alkenes to Alkanes with Ammonnia
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Sonochemically‐Induced Reduction of Alkenes to Alkanes with Ammonnia

Angewandte Chemie International Edition, 2022, Vol.61 (51) [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.202212719

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38
On the road for more efficient biocompatible two-photon excitable fluorophores
On the road for more efficient biocompatible two-photon excitable fluorophores
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On the road for more efficient biocompatible two-photon excitable fluorophores

Chemistry : a European journal, 2022-01 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0947-6539 ;EISSN: 1521-3765 ;DOI: 10.1002/chem.202104378 ;PMID: 35060213

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39
Lysosomal targeting of b-cyclodextrin
Lysosomal targeting of b-cyclodextrin
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Lysosomal targeting of b-cyclodextrin

Chemistry : a European journal, 2022, Vol.29 (4) [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0947-6539 ;EISSN: 1521-3765 ;DOI: 10.1002/chem.202203252

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40
Correction for Llanos et al., Exploration of the chemical space and its three historical regimes
Correction for Llanos et al., Exploration of the chemical space and its three historical regimes
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Correction for Llanos et al., Exploration of the chemical space and its three historical regimes

Proceedings of the National Academy of Sciences - PNAS, 2019-07, Vol.116 (29), p.14779-14779 [Peer Reviewed Journal]

Copyright National Academy of Sciences Jul 16, 2019 ;2019 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.1910465116 ;PMID: 31285350

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