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‘Heteroaromatic Rings of the Future’: Exploration of Unconquered Chemical Space
‘Heteroaromatic Rings of the Future’: Exploration of Unconquered Chemical Space
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‘Heteroaromatic Rings of the Future’: Exploration of Unconquered Chemical Space

Synthesis (Stuttgart), 2019-01, Vol.51 (2), p.384-398 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0039-7881 ;EISSN: 1437-210X ;DOI: 10.1055/s-0037-1611279

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2
1,6-Naphthyridin-7(6 H )-ones: synthesis and optical properties
1,6-Naphthyridin-7(6 H )-ones: synthesis and optical properties
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1,6-Naphthyridin-7(6 H )-ones: synthesis and optical properties

Organic & biomolecular chemistry, 2023-04, Vol.21 (14), p.2976-2982 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1477-0520 ;EISSN: 1477-0539 ;DOI: 10.1039/D3OB00081H

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3
Synthesis, Photophysical Properties, and Living Cell Imaging of Theranostic Half-Sandwich Iridium-4,4-Difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) Dyads
Synthesis, Photophysical Properties, and Living Cell Imaging of Theranostic Half-Sandwich Iridium-4,4-Difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) Dyads
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Synthesis, Photophysical Properties, and Living Cell Imaging of Theranostic Half-Sandwich Iridium-4,4-Difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) Dyads

Organometallics, 2017-09, Vol.36 (18) [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0276-7333 ;EISSN: 1520-6041 ;DOI: 10.1021/acs.organomet.7b00250

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4
Metal-based BODIPY derivatives as multimodal tools for life sciences
Metal-based BODIPY derivatives as multimodal tools for life sciences
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Metal-based BODIPY derivatives as multimodal tools for life sciences

Coordination chemistry reviews, 2018-03, Vol.358, p.108-124 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0010-8545 ;EISSN: 1873-3840 ;DOI: 10.1016/j.ccr.2017.12.007

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5
Synthetic strategy studies for a concise access to functionalized pyrano[4,​3-​b]​pyridin-​7-​ones: An entry to semi-rigid analogs of antihistamines
Synthetic strategy studies for a concise access to functionalized pyrano[4,​3-​b]​pyridin-​7-​ones: An entry to semi-rigid analogs of antihistamines
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Synthetic strategy studies for a concise access to functionalized pyrano[4,​3-​b]​pyridin-​7-​ones: An entry to semi-rigid analogs of antihistamines

European journal of organic chemistry, 2020-09, Vol.2020 (36), p.5880-5889 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1434-193X ;EISSN: 1099-0690 ;DOI: 10.1002/ejoc.202001016

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