Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Torben Rogge"'
Autor:
Zi-Jing Zhang, Shu-Wen Li, João C. A. Oliveira, Yanjun Li, Xinran Chen, Shuo-Qing Zhang, Li-Cheng Xu, Torben Rogge, Xin Hong, Lutz Ackermann
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-9 (2023)
Abstract Challenging enantio- and diastereoselective cobalt-catalyzed C–H alkylation has been realized by an innovative data-driven knowledge transfer strategy. Harnessing the statistics of a related transformation as the knowledge source, the desi
Externí odkaz:
https://doaj.org/article/cc57c98e8eb44e86b9cc7691dc65448f
Autor:
Alexandra Schischko, Nikolaos Kaplaneris, Torben Rogge, Giedre Sirvinskaite, Jongwoo Son, Lutz Ackermann
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-9 (2019)
Palladium-catalyzed late-stage diversification of structurally complex peptides has major shortcomings. Here, the authors developed a ruthenium-catalyzed C–H alkylations of peptides allowing for fluorescence labeling, late-stage diversifications an
Externí odkaz:
https://doaj.org/article/0d0672b6c73c4b54bd92fda2d14eeb00
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-10 (2018)
Chalcogen-containing compounds find broad application in chemical industry. Here, the authors report a nickel-catalyzed reductive chalcogenation of unactivated alkyl bromides with thiosulfonates and selenosulfonates to access a range of unsymmetrical
Externí odkaz:
https://doaj.org/article/5a6a88e661cd4a629ba139e7e843fa3d
Autor:
Jie Li, Korkit Korvorapun, Suman De Sarkar, Torben Rogge, David J. Burns, Svenja Warratz, Lutz Ackermann
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-8 (2017)
Whileortho-selective C-H activation is well explored, general meta-selective methods are rare and often require directing groups that are retained in the final products. Here the authors show that transient imine groups can be used to direct the meta
Externí odkaz:
https://doaj.org/article/07468563c5ad43cb8d7d234c58afb3c4
Publikováno v:
Journal of the American Chemical Society. 145:345-358
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::136c4c4151de23dcaab598578803bb84
https://doi.org/10.1021/jacs.2c10090
https://doi.org/10.1021/jacs.2c10090
Autor:
Peter Bellotti, Torben Rogge, Fritz Paulus, Ranjini Laskar, Nils Rendel, Jiajia Ma, K. N. Houk, Frank Glorius
Publikováno v:
Journal of the American Chemical Society. 144:15662-15671
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::895eee435759fc0ace04b8901f6b6646
https://doi.org/10.1021/jacs.2c05687
https://doi.org/10.1021/jacs.2c05687
Autor:
Runze Mao, Daniel J. Wackelin, Cooper S. Jamieson, Torben Rogge, Shilong Gao, Anuvab Das, Doris Mia Taylor, K. N. Houk, Frances H. Arnold
In nature and synthetic chemistry, stereoselective [2+1] cyclopropanation is the most prevalent strategy for the synthesis of chiral cyclopropanes, a class of key pharmacophores in pharmaceuticals and bioactive natural products. One of the most exten
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac552d0bf48a8e968ace926188b9a4a8
https://doi.org/10.21203/rs.3.rs-2802333/v1
https://doi.org/10.21203/rs.3.rs-2802333/v1
Publikováno v:
Journal of the American Chemical Society.
Hypervalent chloranes are a class of rare and poorly explored reagents. Their unique electronic properties confer reactivity that is complementary to that of the common iodanes and emerging bromanes. Highly chemo- and regioselective, metal-free, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8e20de1e07c96d61819203e418060cb5
https://pubmed.ncbi.nlm.nih.gov/36535642
https://pubmed.ncbi.nlm.nih.gov/36535642
Autor:
Peter, Bellotti, Torben, Rogge, Fritz, Paulus, Ranjini, Laskar, Nils, Rendel, Jiajia, Ma, K N, Houk, Frank, Glorius
Publikováno v:
Journal of the American Chemical Society. 144(34)
Cycloaddition reactions─epitomized by the Diels-Alder reaction─offer an arguably unmatched springboard for achieving chemical complexity, often with excellent selectivity, in a modular single step. We report the synthesis of aza-acenaphthenes in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::eaf9e094d6d799e42fa15e714f2fcabf
https://pubmed.ncbi.nlm.nih.gov/35984989
https://pubmed.ncbi.nlm.nih.gov/35984989
Autor:
Diego Broggini, Torben Rogge, Thomas Müller, Lutz Ackermann, Xiaoyan Hou, Simon Wagschal, Hendrik Simon
Publikováno v:
Synlett. 33:346-350
A triazole-directed direct C–H arylation of arenes with electron-deficient aryl halides or a synthetically useful pyrimidyl chloride was achieved through ruthenium catalysis. Our novel strategy provides operationally simple and environmentally beni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7737a0314bafae760aa545dad209de5
https://doi.org/10.1055/a-1495-6994
https://doi.org/10.1055/a-1495-6994