[{"date_published":"2025-09-26T00:00:00Z","_id":"20537","language":[{"iso":"eng"}],"date_updated":"2025-12-01T15:03:10Z","quality_controlled":"1","year":"2025","month":"09","status":"public","corr_author":"1","title":"Photochemical cross-couplings using semiconducting materials","volume":18,"doi":"10.1055/a-2690-9269","publication_status":"inpress","publication":"Synlett","abstract":[{"lang":"eng","text":"In this personal account, I describe the work performed in my research group on the development of methods that harness heterogeneous photocatalysts for light-mediated nickel-catalyzed cross-couplings. This includes catalytic systems using carbon nitride materials, dye-sensitized TiO₂, covalent organic frameworks (COFs), and conjugated polymers. The rationale behind the selection of materials and how their use led to the identification of catalyst deactivation, structure–activity relationships, and future opportunities is discussed."}],"publication_identifier":{"eissn":["1437-2096"],"issn":["0936-5214"]},"oa_version":"None","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","publisher":"Georg Thieme Verlag","article_type":"original","date_created":"2025-10-26T23:01:35Z","day":"26","intvolume":"        18","type":"journal_article","article_processing_charge":"No","citation":{"chicago":"Pieber, Bartholomäus. “Photochemical Cross-Couplings Using Semiconducting Materials.” <i>Synlett</i>. Georg Thieme Verlag, n.d. <a href=\"https://doi.org/10.1055/a-2690-9269\">https://doi.org/10.1055/a-2690-9269</a>.","ama":"Pieber B. Photochemical cross-couplings using semiconducting materials. <i>Synlett</i>. 18. doi:<a href=\"https://doi.org/10.1055/a-2690-9269\">10.1055/a-2690-9269</a>","short":"B. Pieber, Synlett 18 (n.d.).","ieee":"B. Pieber, “Photochemical cross-couplings using semiconducting materials,” <i>Synlett</i>, vol. 18. Georg Thieme Verlag.","mla":"Pieber, Bartholomäus. “Photochemical Cross-Couplings Using Semiconducting Materials.” <i>Synlett</i>, vol. 18, Georg Thieme Verlag, doi:<a href=\"https://doi.org/10.1055/a-2690-9269\">10.1055/a-2690-9269</a>.","apa":"Pieber, B. (n.d.). Photochemical cross-couplings using semiconducting materials. <i>Synlett</i>. Georg Thieme Verlag. <a href=\"https://doi.org/10.1055/a-2690-9269\">https://doi.org/10.1055/a-2690-9269</a>","ista":"Pieber B. Photochemical cross-couplings using semiconducting materials. Synlett. 18."},"department":[{"_id":"BaPi"}],"external_id":{"isi":["001582268500001"]},"isi":1,"scopus_import":"1","author":[{"full_name":"Pieber, Bartholomäus","last_name":"Pieber","id":"93e5e5b2-0da6-11ed-8a41-af589a024726","orcid":"0000-0001-8689-388X","first_name":"Bartholomäus"}],"OA_type":"closed access"},{"date_created":"2022-08-25T11:52:22Z","month":"01","article_type":"letter_note","publisher":"Georg Thieme Verlag","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","year":"2016","oa_version":"None","publication_identifier":{"eissn":["1437-2096"],"issn":["0936-5214"]},"quality_controlled":"1","language":[{"iso":"eng"}],"date_updated":"2023-02-21T10:10:33Z","date_published":"2016-01-04T00:00:00Z","publication_status":"published","_id":"11988","publication":"Synlett","abstract":[{"text":"A continuous Bucherer–Bergs hydantoin synthesis utilizing intensified conditions is reported. The methodology is characterized by a two-feed flow approach to independently feed the organic substrate and the aqueous reagent solution. The increased interfacial area of the biphasic reaction mixture and the lack of headspace enabled almost quantitative conversions within ca. 30 minutes at 120 °C and 20 bar even for unpolar starting materials. In addition, a selective N(3)-monoalkylation of the resulting heterocycles under batch microwave conditions is reported yielding potential acetylcholinesterase inhibitors.","lang":"eng"}],"doi":"10.1055/s-0035-1560317","extern":"1","author":[{"full_name":"Kappe, C.","last_name":"Kappe","first_name":"C."},{"first_name":"Julia","full_name":"Monteiro, Julia","last_name":"Monteiro"},{"full_name":"Pieber, Bartholomäus","last_name":"Pieber","first_name":"Bartholomäus","id":"93e5e5b2-0da6-11ed-8a41-af589a024726","orcid":"0000-0001-8689-388X"},{"first_name":"Arlene","full_name":"Corrêa, Arlene","last_name":"Corrêa"}],"volume":27,"title":"Continuous synthesis of hydantoins: Intensifying the Bucherer–Bergs reaction","scopus_import":"1","issue":"01","citation":{"ieee":"C. Kappe, J. Monteiro, B. Pieber, and A. Corrêa, “Continuous synthesis of hydantoins: Intensifying the Bucherer–Bergs reaction,” <i>Synlett</i>, vol. 27, no. 01. Georg Thieme Verlag, pp. 83–87, 2016.","mla":"Kappe, C., et al. “Continuous Synthesis of Hydantoins: Intensifying the Bucherer–Bergs Reaction.” <i>Synlett</i>, vol. 27, no. 01, Georg Thieme Verlag, 2016, pp. 83–87, doi:<a href=\"https://doi.org/10.1055/s-0035-1560317\">10.1055/s-0035-1560317</a>.","apa":"Kappe, C., Monteiro, J., Pieber, B., &#38; Corrêa, A. (2016). Continuous synthesis of hydantoins: Intensifying the Bucherer–Bergs reaction. <i>Synlett</i>. Georg Thieme Verlag. <a href=\"https://doi.org/10.1055/s-0035-1560317\">https://doi.org/10.1055/s-0035-1560317</a>","ista":"Kappe C, Monteiro J, Pieber B, Corrêa A. 2016. Continuous synthesis of hydantoins: Intensifying the Bucherer–Bergs reaction. Synlett. 27(01), 83–87.","chicago":"Kappe, C., Julia Monteiro, Bartholomäus Pieber, and Arlene Corrêa. “Continuous Synthesis of Hydantoins: Intensifying the Bucherer–Bergs Reaction.” <i>Synlett</i>. Georg Thieme Verlag, 2016. <a href=\"https://doi.org/10.1055/s-0035-1560317\">https://doi.org/10.1055/s-0035-1560317</a>.","ama":"Kappe C, Monteiro J, Pieber B, Corrêa A. Continuous synthesis of hydantoins: Intensifying the Bucherer–Bergs reaction. <i>Synlett</i>. 2016;27(01):83-87. doi:<a href=\"https://doi.org/10.1055/s-0035-1560317\">10.1055/s-0035-1560317</a>","short":"C. Kappe, J. Monteiro, B. Pieber, A. Corrêa, Synlett 27 (2016) 83–87."},"page":"83-87","article_processing_charge":"No","type":"journal_article","intvolume":"        27","status":"public","day":"04"},{"publication":"Synlett","abstract":[{"lang":"eng","text":"We report a method for preparing electrode–molecule–electrode junctions that incorporate nonsymmetrical azobenzene dithiols. Our approach is based on sequential deprotection of thiol moieties originally carrying two different protecting groups. The azobenzene derivatives retained their switching properties within monolayers and permitted the photocontrol of electrical conductance."}],"publication_status":"published","extern":"1","doi":"10.1055/s-0033-1340087","publication_identifier":{"eissn":["1437-2096"],"issn":["0936-5214"]},"oa_version":"None","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","date_created":"2023-08-01T09:47:17Z","publisher":"Georg Thieme Verlag","article_type":"original","intvolume":"        24","day":"22","keyword":["Organic Chemistry"],"citation":{"ieee":"T. Ely <i>et al.</i>, “Photocontrol of electrical conductance with a nonsymmetrical azobenzene dithiol,” <i>Synlett</i>, vol. 24, no. 18. Georg Thieme Verlag, pp. 2370–2374, 2013.","mla":"Ely, Tal, et al. “Photocontrol of Electrical Conductance with a Nonsymmetrical Azobenzene Dithiol.” <i>Synlett</i>, vol. 24, no. 18, Georg Thieme Verlag, 2013, pp. 2370–74, doi:<a href=\"https://doi.org/10.1055/s-0033-1340087\">10.1055/s-0033-1340087</a>.","apa":"Ely, T., Das, S., Li, W., Kundu, P., Tirosh, E., Cahen, D., … Klajn, R. (2013). Photocontrol of electrical conductance with a nonsymmetrical azobenzene dithiol. <i>Synlett</i>. Georg Thieme Verlag. <a href=\"https://doi.org/10.1055/s-0033-1340087\">https://doi.org/10.1055/s-0033-1340087</a>","ista":"Ely T, Das S, Li W, Kundu P, Tirosh E, Cahen D, Vilan A, Klajn R. 2013. Photocontrol of electrical conductance with a nonsymmetrical azobenzene dithiol. Synlett. 24(18), 2370–2374.","chicago":"Ely, Tal, Sanjib Das, Wenjie Li, Pintu Kundu, Einat Tirosh, David Cahen, Ayelet Vilan, and Rafal Klajn. “Photocontrol of Electrical Conductance with a Nonsymmetrical Azobenzene Dithiol.” <i>Synlett</i>. Georg Thieme Verlag, 2013. <a href=\"https://doi.org/10.1055/s-0033-1340087\">https://doi.org/10.1055/s-0033-1340087</a>.","ama":"Ely T, Das S, Li W, et al. Photocontrol of electrical conductance with a nonsymmetrical azobenzene dithiol. <i>Synlett</i>. 2013;24(18):2370-2374. doi:<a href=\"https://doi.org/10.1055/s-0033-1340087\">10.1055/s-0033-1340087</a>","short":"T. Ely, S. Das, W. Li, P. Kundu, E. Tirosh, D. Cahen, A. Vilan, R. Klajn, Synlett 24 (2013) 2370–2374."},"type":"journal_article","article_processing_charge":"No","issue":"18","author":[{"first_name":"Tal","full_name":"Ely, Tal","last_name":"Ely"},{"full_name":"Das, Sanjib","last_name":"Das","first_name":"Sanjib"},{"first_name":"Wenjie","full_name":"Li, Wenjie","last_name":"Li"},{"first_name":"Pintu","last_name":"Kundu","full_name":"Kundu, Pintu"},{"first_name":"Einat","last_name":"Tirosh","full_name":"Tirosh, Einat"},{"first_name":"David","full_name":"Cahen, David","last_name":"Cahen"},{"full_name":"Vilan, Ayelet","last_name":"Vilan","first_name":"Ayelet"},{"id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b","first_name":"Rafal","full_name":"Klajn, Rafal","last_name":"Klajn"}],"scopus_import":"1","_id":"13405","date_published":"2013-10-22T00:00:00Z","quality_controlled":"1","language":[{"iso":"eng"}],"date_updated":"2024-10-14T12:21:03Z","year":"2013","month":"10","status":"public","page":"2370-2374","volume":24,"title":"Photocontrol of electrical conductance with a nonsymmetrical azobenzene dithiol"},{"title":"Simple synthesis of 2-substituted Tetrahydrofuran-3-carbonitriles","volume":2000,"status":"public","page":"1773-1774","year":"2000","month":"12","date_published":"2000-12-01T00:00:00Z","_id":"13437","date_updated":"2023-08-02T07:54:46Z","language":[{"iso":"eng"}],"quality_controlled":"1","issue":"12","scopus_import":"1","author":[{"first_name":"Mieczysław","full_name":"Macogonkosza, Mieczysław","last_name":"Macogonkosza"},{"full_name":"Przyborowski, Jacek","last_name":"Przyborowski","first_name":"Jacek"},{"last_name":"Klajn","full_name":"Klajn, Rafal","first_name":"Rafal","id":"8e84690e-1e48-11ed-a02b-a1e6fb8bb53b"},{"full_name":"Kwast, Andrzej","last_name":"Kwast","first_name":"Andrzej"}],"keyword":["Organic Chemistry"],"day":"01","intvolume":"      2000","article_processing_charge":"No","type":"journal_article","citation":{"ieee":"M. Macogonkosza, J. Przyborowski, R. Klajn, and A. Kwast, “Simple synthesis of 2-substituted Tetrahydrofuran-3-carbonitriles,” <i>Synlett</i>, vol. 2000, no. 12. Georg Thieme Verlag, pp. 1773–1774, 2000.","apa":"Macogonkosza, M., Przyborowski, J., Klajn, R., &#38; Kwast, A. (2000). Simple synthesis of 2-substituted Tetrahydrofuran-3-carbonitriles. <i>Synlett</i>. Georg Thieme Verlag. <a href=\"https://doi.org/10.1055/s-2000-8670\">https://doi.org/10.1055/s-2000-8670</a>","ista":"Macogonkosza M, Przyborowski J, Klajn R, Kwast A. 2000. Simple synthesis of 2-substituted Tetrahydrofuran-3-carbonitriles. Synlett. 2000(12), 1773–1774.","mla":"Macogonkosza, Mieczysław, et al. “Simple Synthesis of 2-Substituted Tetrahydrofuran-3-Carbonitriles.” <i>Synlett</i>, vol. 2000, no. 12, Georg Thieme Verlag, 2000, pp. 1773–74, doi:<a href=\"https://doi.org/10.1055/s-2000-8670\">10.1055/s-2000-8670</a>.","chicago":"Macogonkosza, Mieczysław, Jacek Przyborowski, Rafal Klajn, and Andrzej Kwast. “Simple Synthesis of 2-Substituted Tetrahydrofuran-3-Carbonitriles.” <i>Synlett</i>. Georg Thieme Verlag, 2000. <a href=\"https://doi.org/10.1055/s-2000-8670\">https://doi.org/10.1055/s-2000-8670</a>.","ama":"Macogonkosza M, Przyborowski J, Klajn R, Kwast A. Simple synthesis of 2-substituted Tetrahydrofuran-3-carbonitriles. <i>Synlett</i>. 2000;2000(12):1773-1774. doi:<a href=\"https://doi.org/10.1055/s-2000-8670\">10.1055/s-2000-8670</a>","short":"M. Macogonkosza, J. Przyborowski, R. Klajn, A. Kwast, Synlett 2000 (2000) 1773–1774."},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","article_type":"letter_note","publisher":"Georg Thieme Verlag","date_created":"2023-08-01T10:39:48Z","doi":"10.1055/s-2000-8670","extern":"1","publication_status":"published","abstract":[{"text":"Liquid/liquid Phase Transfer Catalysis (PTC) reaction of 4-chlorobutyronitrile with nonenolisable aldehydes leads via an addition-cyclisation reaction sequence to derivatives of tetrahydrofuran-3-carbonitrile.","lang":"eng"}],"publication":"Synlett","publication_identifier":{"eissn":["1437-2096"],"issn":["0936-5214"]},"oa_version":"None"}]