Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Santeri Alfred Arttu Aikonen"'
Autor:
Stefan Taubert, Mikko Muuronen, Tao Hu, Dage Sundholm, Tom Wirtanen, David Sebastian Casadio, Anna Lenarda, Santeri Alfred Arttu Aikonen, Martin Nieger, Juho Helaja
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
Mildly thermal air or HNO3 oxidized activated carbons catalyse oxidative dehydrogenative couplings of benzo[b]fused heteroaryl 2,2’‐dimers, e.g., 2‐(benzofuran‐2‐yl)‐1H‐indole, to chiral 3,3’‐coupled cyclooctatetraenes or carbazole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::477f63f87dae22dfe7158d60765503ad
https://doi.org/10.1002/chem.202005433
https://doi.org/10.1002/chem.202005433
Autor:
Tanja Kallio, Fatemeh Davodi, Tom Wirtanen, Michele Melchionna, Mikko Muuronen, Juho Helaja, Marianna Kemell, Tao Hu, Santeri Alfred Arttu Aikonen
Publikováno v:
Chemistry – A European Journal. 25:12288-12293
HNO3-oxidized carbon nanotubes catalyze oxidative dehydrogenative (ODH) carbon-carbon bond formation between electron-rich (hetero)aryls with O-2 as a terminal oxidant. The recyclable carbocatalytic method provides a convenient and an operationally e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3fda05e54c3ef38f01c8fbd4ceda641
https://doi.org/10.1002/chem.201903054
https://doi.org/10.1002/chem.201903054
Publikováno v:
Organic Letters
A photoreductive protocol utilizing [Ru-(bpy)3]2+ photocatalyst, blue light LEDs, and ascorbic acid(AscH2) has been developed to reduce nitro N-heteroaryls to the corresponding anilines. Based on experimental and computational results and previous st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b3971fc9c52fda435b69bd94224d30e
https://doi.org/10.1021/acs.orglett.9b01205
https://doi.org/10.1021/acs.orglett.9b01205
Autor:
Lucília S. Ribeiro, Juho Helaja, Sami Hietala, Tao Hu, Tom Wirtanen, Lukas Enders, Manuel Fernando R. Pereira, David Sebastian Casadio, Santeri Alfred Arttu Aikonen, Anna Lenarda
A simple "reagent-free" thermal air treatment turns active carbon into a mildly oxidized material with increased quinoidic content that catalytically dehydrogenates saturated N-heterocycles to the corresponding aromatic compounds. Thermal decarboxyla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e86636032f56777ca210b176b1f3881c
https://hdl.handle.net/10216/136378
https://hdl.handle.net/10216/136378
Autor:
Santeri Alfred Arttu Aikonen
Publikováno v:
University of Helsinki
Reaction mechanisms play an integral part in understanding chemical phenomena. Chemists use their knowledge of reaction mechanisms both when formulating research questions and when carrying out experiments in the fume hood or in silico. Accurate unde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::d24db2e7614e0dbd1cc8d670ce8d49e1
http://hdl.handle.net/10138/321054
http://hdl.handle.net/10138/321054
Autor:
Mikko Muuronen, Jordi Burés, Otto Seppänen, Santeri Alfred Arttu Aikonen, Carla Alamillo-Ferrer, Juho Helaja
Publikováno v:
Seppänen, O, Aikonen, S, Muuronen, M, Alamillo-ferrer, C, Burés, J & Helaja, J 2020, ' Dual H-bond activation of NHC–Au(I)–Cl complexes with amide functionalized side-arms assisted by H-bond donor substrates or acid additives ', Chemical Communications, vol. 56, no. 93, pp. 14697-14700 . https://doi.org/10.1039/D0CC05999D
Novel approach with amide-tethered H-bond donor NHC ligands enabled Au(I)-catalysis via H-bonding. The plain NHC-Au(I)-Cl complex catalysed conversions of terminal N-propynamides to oxazolines, and enyne cycloisomerization with an acid additive, in D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6676c59d62304d00d9204d6f82ce5af6
https://pubmed.ncbi.nlm.nih.gov/33169740
https://pubmed.ncbi.nlm.nih.gov/33169740
Autor:
Jordi Burés, Tom Wirtanen, Juho Helaja, Santeri Alfred Arttu Aikonen, Sami Heikkinen, Mikko Muuronen, Joshua Musgreave
Publikováno v:
Aikonen, S, Muuronen, M, Wirtanen, T, Heikkinen, S, Musgreave, J, Bures Amat, J & Helaja, J 2018, ' Gold(I)-catalyzed 1,3-O-transposition of ynones: Mechanism and catalytic acceleration with electron rich aldehydes ', ACS Catalysis, vol. 8, pp. 960-967 . https://doi.org/10.1021/acscatal.7b04262
The gold-catalyzed 1,3-O-transposition of ynones occurs intermolecularly via a cyclic organo-gold acetal intermediate formed from the nucleophilic oxo attack of a second ynone, i.e. either starting material or product, on a gold-activated ynone. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1406e9c4f6e6a0b3d8859e868953e88
https://doi.org/10.1021/acscatal.7b04262
https://doi.org/10.1021/acscatal.7b04262