Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Arumugam, Jayaraman"'
Publikováno v:
ACS Omega, Vol 2, Iss 11, Pp 7849-7861 (2017)
Externí odkaz:
https://doaj.org/article/337ae9fa84144005a099832aef3f2f53
Autor:
Debabrata Dhara, Arumugam Jayaraman, Marcel Härterich, Merle Arrowsmith, Malte Jürgensen, Maximilian Michel, Holger Braunschweig
Publikováno v:
Chemistry – A European Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9408991904856cf1989c738d53e186b2
https://doi.org/10.1002/chem.202300483
https://doi.org/10.1002/chem.202300483
Autor:
Alexander Okorn, Arumugam Jayaraman, Lukas Englert, Merle Arrowsmith, Theresa Swoboda, Jeanette Weigelt, Carina Brunecker, Merlin Hess, Anna Lamprecht, Carsten Lenczyk, Maximilian Rang, Holger Braunschweig
Publikováno v:
Chemical Science. 13:7566-7574
In contrast to classical B–B bond-centred diborene hydrogenation, polycyclic aromatic hydrocarbon-substituted diborenes first undergo thermal intramolecular hydroarylation, followed by hydrogenation of the remaining B–B and endocyclic B–C bonds
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed30d3add43c3867eb353bd167043a18
https://doi.org/10.1039/d2sc02515a
https://doi.org/10.1039/d2sc02515a
Autor:
Stephanie Kachel, Arumugam Jayaraman, Alexander Okorn, Ivo Krummenacher, Regina Drescher, Carina Brunecker, Sonja Fuchs, Merlin Heß, Tom E. Stennett, Holger Braunschweig
Publikováno v:
Chemical Communications. 58:2331-2334
Unprecedented direct indole formation from the thermal reaction of an electron-rich alkyne with aryl azides has been discovered, involving triazole-derived imino carbenes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e83d2156c12319058fe1acf58464ea1
https://doi.org/10.1039/d1cc06975f
https://doi.org/10.1039/d1cc06975f
Autor:
Ramapada Dolai, Rahul Kumar, Benedict J. Elvers, Pradeep Kumar Pal, Benson Joseph, Rina Sikari, Mithilesh Kumar Nayak, Avijit Maiti, Tejender Singh, Nicolas Chrysochos, Arumugam Jayaraman, Ivo Krummenacher, Jagannath Mondal, U. Deva Priyakumar, Holger Braunschweig, Cem B. Yildiz, Carola Schulzke, Anukul Jana
Publikováno v:
Chemistry – A European Journal. 29
Herein, a new type of carbodicarbene (CDC) comprising two different classes of carbenes is reported; NHC and CAAC as donor substituents and compare the molecular structure and coordination to Au(I)Cl to those of NHC-only and CAAC-only analogues. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5c023634b888365b4a1892c6ed55619
https://doi.org/10.1002/chem.202202888
https://doi.org/10.1002/chem.202202888
Autor:
Alexandra Friedrich, Todd B. Marder, Udo Radius, Florian Kerner, Arumugam Jayaraman, Yudha P. Budiman
Publikováno v:
Journal of the American Chemical Society. 142:6036-6050
C–C reductive elimination from [PdL2(C6F5)2] to form polyfluorinated biaryls has been a challenge for over 50 years. Thus, palladium-catalyzed homocoupling of arylboronates (ArF–Bpin) containing tw...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1a70956abddaf730f7b0bb938870175
https://doi.org/10.1021/jacs.9b11871
https://doi.org/10.1021/jacs.9b11871
Autor:
Sonja Fuchs, Arumugam Jayaraman, Ivo Krummenacher, Laura Haley, Marta Baštovanović, Maximilian Fest, Krzysztof Radacki, Holger Helten, Holger Braunschweig
Publikováno v:
Chemical science. 13(10)
We report that the outcome of the tin-boron exchange reaction of a mixed thiophene-benzo-fused stannole with aryldibromoboranes is associated with the steric bulk of the aryl substituent of the borane reagent, leading to either boroles or large dibor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe78285de04d833fc62bf228b4cf427d
https://pubmed.ncbi.nlm.nih.gov/35382462
https://pubmed.ncbi.nlm.nih.gov/35382462
Autor:
Wei Lu, Arumugam Jayaraman, Felipe Fantuzzi, Rian D. Dewhurst, Marcel Härterich, Maximilian Dietz, Stephan Hagspiel, Ivo Krummenacher, Kai Hammond, Jingjing Cui, Holger Braunschweig
Publikováno v:
Angewandte Chemie. 134
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2b3f8e7ff1f5a6dd4e56fd421b5f47a
https://doi.org/10.1002/ange.202113947
https://doi.org/10.1002/ange.202113947
Autor:
Stephan Hagspiel, Kai Hammond, Marcel Härterich, Ivo Krummenacher, Wei Lu, Jingjing Cui, Arumugam Jayaraman, Maximilian Dietz, Felipe Fantuzzi, Rian D. Dewhurst, Holger Braunschweig
Publikováno v:
Angewandte Chemie (International ed. in English). 61(3)
A one-pot synthesis of a CAAC-stabilized, unsymmetrical, cyclic diborene was achieved via consecutive two-electron reduction steps from an adduct of CAAC and B\(_2\)Br\(_4\)(SMe\(_2\))\(_2\). Theoretical studies revealed that this diborene has a cons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aca94c3bb1c767a361d7fe6b333550f6
https://pubmed.ncbi.nlm.nih.gov/34750945
https://pubmed.ncbi.nlm.nih.gov/34750945
Publikováno v:
Organometallics. 37:4699-4710
While alkyne insertion into metal–carbon(sp2) bonds is common in transition metal chemistry, direct alkyne insertions into E–C(sp2) bonds are very rare in main group chemistry. Herein, we report a direct alkyne insertion reaction into the P–C(a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a77120d1bb73690f77966b5caf870ae
https://doi.org/10.1021/acs.organomet.8b00718
https://doi.org/10.1021/acs.organomet.8b00718