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Bromine radical release from a nickel-complex facilitates the activation of alkyl boronic acids: a boron selective Suzuki-Miyaura cross coupling.

Autor: Oliva M; Laboratory for Organic & Microwave-Assisted Chemistry (LOMAC), Department of Chemistry, University of Leuven (KU Leuven) Celestijnenlaan 200F B-3001 Leuven Belgium., Pillitteri S; Laboratory for Organic & Microwave-Assisted Chemistry (LOMAC), Department of Chemistry, University of Leuven (KU Leuven) Celestijnenlaan 200F B-3001 Leuven Belgium., Schörgenhumer J; Department of Chemistry, University of Zurich Winterthurerstrasse 190 CH-8057 Zurich Switzerland., Saito R; Department of Chemistry and Centre for Sustainable Chemistry, Ghent University Krijgslaan 281 (S3) 9000 Ghent Belgium., Van der Eycken EV; Laboratory for Organic & Microwave-Assisted Chemistry (LOMAC), Department of Chemistry, University of Leuven (KU Leuven) Celestijnenlaan 200F B-3001 Leuven Belgium.; Peoples' Friendship University of Russia (RUDN University) Miklukho-Maklaya Street 6 117198 Moscow Russia., Sharma UK; Laboratory for Organic & Microwave-Assisted Chemistry (LOMAC), Department of Chemistry, University of Leuven (KU Leuven) Celestijnenlaan 200F B-3001 Leuven Belgium.; Department of Chemistry and Biochemistry, University of Missouri-St. Louis, One University Boulevard St. Louis MO 63121 USA sharmauk@umsl.edu.

Publikováno v: Chemical science [Chem Sci] 2024 Sep 26. Date of Electronic Publication: 2024 Sep 26.

Hydroalkylation of styrenes enabled by boryl radical mediated halogen atom transfer.

Autor: Pillitteri S; Laboratory for Organic & Microwave-Assisted Chemistry (LOMAC), Department of Chemistry, University of Leuven (KU Leuven) Celestijnenlaan 200F B-3001 Leuven Belgium upendrakumar.sharma@kuleuven.be usharma81@gmail.com., Walia R; Department of Chemistry, The University of Hong Kong Pokfulam Road Hong Kong SAR.; Department of Chemistry, City University of Hong Kong Tat Chee Avenue Kowloon Hong Kong SAR., Van der Eycken EV; Laboratory for Organic & Microwave-Assisted Chemistry (LOMAC), Department of Chemistry, University of Leuven (KU Leuven) Celestijnenlaan 200F B-3001 Leuven Belgium upendrakumar.sharma@kuleuven.be usharma81@gmail.com.; Peoples' Friendship University of Russia (RUDN University) Miklukho-Maklaya Street 6 117198 Moscow Russia., Sharma UK; Laboratory for Organic & Microwave-Assisted Chemistry (LOMAC), Department of Chemistry, University of Leuven (KU Leuven) Celestijnenlaan 200F B-3001 Leuven Belgium upendrakumar.sharma@kuleuven.be usharma81@gmail.com.

Publikováno v: Chemical science [Chem Sci] 2024 May 03; Vol. 15 (23), pp. 8813-8819. Date of Electronic Publication: 2024 May 03 (Print Publication: 2024).

Divergent and Nucleophile-Assisted Rearrangement in the Construction of Pyrrolo[2,1-b][3]benzazepine and Pyrido[2,1-a]isoquinoline Scaffolds.

Autor: Obydennik AY; Organic Chemistry Department, Science Faculty, Рeoples' Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya St, Moscow, 117198, Russian Federation., Titov AA; Organic Chemistry Department, Science Faculty, Рeoples' Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya St, Moscow, 117198, Russian Federation., Listratova AV; Organic Chemistry Department, Science Faculty, Рeoples' Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya St, Moscow, 117198, Russian Federation., Borisova TN; Organic Chemistry Department, Science Faculty, Рeoples' Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya St, Moscow, 117198, Russian Federation., Sokolova IL; Organic Chemistry Department, Science Faculty, Рeoples' Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya St, Moscow, 117198, Russian Federation., Rybakov VB; Department of Chemistry, Lomonosov Moscow State University, Leninskie Gory, 1-3, Moscow, 119991, Russian Federation., Van der Eycken EV; Organic Chemistry Department, Science Faculty, Рeoples' Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya St, Moscow, 117198, Russian Federation.; Laboratory for Organic & Microwave-Assisted Chemistry (LOMAC), Department of Chemistry, University of Leuven (KU Leuven), Celestijnenlaan 200F, Leuven, 3001, Belgium., Voskressensky LG; Organic Chemistry Department, Science Faculty, Рeoples' Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya St, Moscow, 117198, Russian Federation., Varlamov AV; Organic Chemistry Department, Science Faculty, Рeoples' Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya St, Moscow, 117198, Russian Federation.

Publikováno v: Chemistry (Weinheim an der Bergstrasse, Germany) [Chemistry] 2024 Jan 11; Vol. 30 (3), pp. e202302919. Date of Electronic Publication: 2023 Nov 20.

Application of Metal-Free Dearomatization Reaction as a Sustainable Strategy to Direct Access Complex Cyclic Compounds.

Autor: Xu X; Department of Chemistry, KU Leuven, Celestijnenlaan 200F, Leuven, 3001, Belgium., Zhong L; College of Chemistry and Chemical Engineering, Shanghai University of Engineering Science, Shanghai, 201620, China., Feng H; College of Chemistry and Chemical Engineering, Shanghai University of Engineering Science, Shanghai, 201620, China.; Shanghai Frontiers Science Research Center for Druggability of Cardiovascular Noncoding RNA, Shanghai University of Engineering Science, Shanghai, 201620, China., Van der Eycken EV; Department of Chemistry, KU Leuven, Celestijnenlaan 200F, Leuven, 3001, Belgium.; Peoples' Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya Street, Moscow, 117198, Russia.

Publikováno v: Chemical record (New York, N.Y.) [Chem Rec] 2023 Oct; Vol. 23 (10), pp. e202300101. Date of Electronic Publication: 2023 May 02.