Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Alexander B. Dürr"'
Autor:
Matthew A. Horwitz, Alexander B. Dürr, Konstantinos Afratis, Zijun Chen, Julia Soika, Kirsten E. Christensen, Makoto Fushimi, Robert S. Paton, Véronique Gouverneur
Publikováno v:
Journal of the American Chemical Society. 145:9708-9717
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91a81d6f5611ba1a3bed5d3f4539e28b
https://doi.org/10.1021/jacs.3c01303
https://doi.org/10.1021/jacs.3c01303
Autor:
Fernanda Duarte, Alistair J. Sterling, Edward A. Anderson, Alexander B. Dürr, Russell C. Smith
Publikováno v:
Chemical Science
[1.1.1]Propellane is the ubiquitous precursor to bicyclo[1.1.1]pentanes (BCPs), motifs of high value in pharmaceutical and materials research. The classical Lewis representation of this molecule places an inter-bridgehead C–C bond along its central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37e05336f8901ed4c86d7295098f7343
https://pubmed.ncbi.nlm.nih.gov/34122945
https://pubmed.ncbi.nlm.nih.gov/34122945
Publikováno v:
Angewandte Chemie (International Ed. in English)
Angewandte Chemie International Edition
Angewandte Chemie International Edition
We herein showcase the ability of NHC-derived dinuclear Ni(I)-Ni(I) complexes to override fundamental reactivity limits of mononuclear (NHC)Ni(0) catalysts in cross-coupling. This is demonstrated with the development of a chemoselective Ni(I) dimer-c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::997507fe85a8cddf7e9c1d2313b5fb9b
https://doi.org/10.1002/anie.201706423
https://doi.org/10.1002/anie.201706423
Autor:
Dimitri F. J. Caputo, Edward A. Anderson, Antonia F. Stepan, Alexander B. Dürr, Carlos Arróniz, James J. Mousseau, Steven J. Mansfield
Publikováno v:
Chemical Science
A wide range of halogenated bicyclo[1.1.1]pentanes are accessed by functional group tolerant radical ring-opening of tricyclo[1.1.1.01,3]pentane, using triethylborane as initiator.
Bicyclo[1.1.1]pentanes (BCPs) are important bioisosteres of 1,4-
Bicyclo[1.1.1]pentanes (BCPs) are important bioisosteres of 1,4-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f91e7a34d17262306f648cf2ff32d27
https://pubmed.ncbi.nlm.nih.gov/29997886
https://pubmed.ncbi.nlm.nih.gov/29997886
Autor:
Kristina Deckers, Pankaj Chauhan, Lucas Mertens, Nico Seling, Daniel Hack, Dieter Enders, Alexander B. Dürr, Gerhard Raabe, Franziska Schoenebeck, Lukas Rübenach
Publikováno v:
Angewandte Chemie 128(5), 1829-1832 (2016). doi:10.1002/ange.201510602
Angewandte Chemie (International Ed. in English)
Angewandte Chemie / International edition 55(5), 1797-1800 (2016). doi:10.1002/anie.201510602
Angewandte Chemie (International Ed. in English)
Angewandte Chemie / International edition 55(5), 1797-1800 (2016). doi:10.1002/anie.201510602
A stereoselective one-pot synthesis of spiropyrazolones through an organocatalytic asymmetric Michael addition and a formal Conia-ene reaction has been developed. Depending on the nitroalkene, the 5-exo-dig-cyclization could be achieved by silver-cat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2af67facd076fbdd6af92cfd2038bc8b
https://publications.rwth-aachen.de/record/567352
https://publications.rwth-aachen.de/record/567352
Publikováno v:
Chemical Science
A computationally guided development of the first efficient protocol to trifluoromethylthiolate aryl and vinyl Csp2–O bonds is presented, showcasing important reactivity requirements for the introduction of potentially reactive functional groups un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::df18c02eec8a98fe6f26e041b39183bd
https://pubmed.ncbi.nlm.nih.gov/29081943
https://pubmed.ncbi.nlm.nih.gov/29081943