Accessing five- and seven-membered phosphorus-based heterocycles via cycloaddition reactions of azophosphines.

Autor: Calder EDE; School of Chemistry, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK. a.jupp@bham.ac.uk., Male L; School of Chemistry, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK. a.jupp@bham.ac.uk., Jupp AR; School of Chemistry, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK. a.jupp@bham.ac.uk.

Publikováno v: Dalton transactions (Cambridge, England : 2003) [Dalton Trans] 2024 Sep 18; Vol. 53 (36), pp. 15032-15039. Date of Electronic Publication: 2024 Sep 18.

Tuning the Electronic Properties of Azophosphines as Ligands and Their Application in Base-Free Transfer Hydrogenation Catalysis.

Autor: Jordan EJ; School of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom., Calder EDE; School of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom., Greene BL; School of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom., Adcock HV; School of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom., Male L; School of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom., Davies PW; School of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom., Jupp AR; School of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom.

Publikováno v: Organometallics [Organometallics] 2024 Sep 06; Vol. 43 (20), pp. 2674-2685. Date of Electronic Publication: 2024 Sep 06 (Print Publication: 2024).

Carbamoylphosphinidene: A Phosphorus Analogue of Carbonyl Nitrene.

Autor: Lu B; Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, 200433 Shanghai, China., Jiang J; Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, 200433 Shanghai, China., Wang L; Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, 200433 Shanghai, China., Jupp AR; Department of Chemistry, Chemistry Research Laboratory, University of Oxford, Mansfield Road, Oxford OX1 3TA, U.K.; School of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT, U.K., Goicoechea JM; Department of Chemistry, Chemistry Research Laboratory, University of Oxford, Mansfield Road, Oxford OX1 3TA, U.K.; Department of Chemistry, Indiana University, 800 East Kirkwood Ave., Bloomington, Indiana 47405, United States., Liu S; LIFM, IGCME, School of Chemistry, Sun Yat-Sen University, 510006 Guangzhou, China., Li Z; LIFM, IGCME, School of Chemistry, Sun Yat-Sen University, 510006 Guangzhou, China., Zhou M; Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, 200433 Shanghai, China., Zeng X; Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, 200433 Shanghai, China.

Publikováno v: Journal of the American Chemical Society [J Am Chem Soc] 2024 Jul 10; Vol. 146 (27), pp. 18699-18705. Date of Electronic Publication: 2024 Jun 29.

Synthesis and Reactivity of the [NCCCO] ^- Cyanoketenate Anion.

Autor: Wang T; School of Chemical Science and Engineering, Tongji University, 1239 Siping Rd, Shanghai, China, 200092., Guo Z; School of Chemical Science and Engineering, Tongji University, 1239 Siping Rd, Shanghai, China, 200092., English LE; School of Chemistry, University of Birmingham, Edgbaston, Birmingham, West Midlands, UK, B15 2TT., Stephan DW; Department of Chemistry, University of Toronto, 80 St. George St., Toronto, Ontario, Canada, M5S3H6., Jupp AR; School of Chemistry, University of Birmingham, Edgbaston, Birmingham, West Midlands, UK, B15 2TT., Xu M; School of Chemical Science and Engineering, Tongji University, 1239 Siping Rd, Shanghai, China, 200092.

Publikováno v: Angewandte Chemie (International ed. in English) [Angew Chem Int Ed Engl] 2024 May 13; Vol. 63 (20), pp. e202402728. Date of Electronic Publication: 2024 Apr 09.

Frustrated Lewis pair catalyzed hydrodehalogenation of benzyl-halides.

Autor: Wang T; Department of Chemistry, University of Toronto, 80 St. George St, Toronto, ON, M5S3H6, Canada. dstephan@chem.utoronto.ca.; College of Chemistry, Faculty of Chemical, Environmental and Biological Science and Technology, Dalian University of Technology, Dalian 116023, China., Xu M; Department of Chemistry, University of Toronto, 80 St. George St, Toronto, ON, M5S3H6, Canada. dstephan@chem.utoronto.ca., Jupp AR; Department of Chemistry, University of Toronto, 80 St. George St, Toronto, ON, M5S3H6, Canada. dstephan@chem.utoronto.ca., Chen SM; Department of Chemistry, University of Toronto, 80 St. George St, Toronto, ON, M5S3H6, Canada. dstephan@chem.utoronto.ca., Qu ZW; Mulliken Center for Theoretical Chemistry, University of Bonn, Beringstrasse 4, Bonn 53115, Germany. qu@thch.uni-bonn.de., Grimme S; Mulliken Center for Theoretical Chemistry, University of Bonn, Beringstrasse 4, Bonn 53115, Germany. qu@thch.uni-bonn.de., Stephan DW; Department of Chemistry, University of Toronto, 80 St. George St, Toronto, ON, M5S3H6, Canada. dstephan@chem.utoronto.ca.

Publikováno v: Chemical communications (Cambridge, England) [Chem Commun (Camb)] 2022 Jan 25; Vol. 58 (8), pp. 1175-1178. Date of Electronic Publication: 2022 Jan 25.