Zobrazeno 1 - 10
of 348
pro vyhledávání: '"Thomas J. Emge"'
Publikováno v:
Inorganic Chemistry. 62:4525-4532
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4625c2227b6366a14bbee158ea5d2e3c
https://doi.org/10.1021/acs.inorgchem.2c04416
https://doi.org/10.1021/acs.inorgchem.2c04416
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 2002-2011 (2018)
Chiral bisoxazoline ligands containing naphthyridine, pyridazine, pyrazole, and phenol bridging units were prepared and shown to form bimetallic complexes with various metal salts. X-ray crystal structures of bis-nickel naphthyridine-bridged, bis-zin
Externí odkaz:
https://doaj.org/article/b843496beca849ef88f2a6286314b9d6
Publikováno v:
Molecules, Vol 27, Iss 1, p 66 (2021)
The amidation reaction of a tetrahydroisoquinolin-1-one-4-carboxylic acid is a key step in the multi-kilogram-scale preparation of the antimalarial drug SJ733, now in phase 2 clinical trials. In the course of investigating THIQ carboxamidations, we f
Externí odkaz:
https://doaj.org/article/ff737fc200354e469dac81ac86464c08
Controlling electronic coupling between two or more redox sites is of interest for tuning the electronic properties of molecules and materials. While classic mixed-valence (MV) systems are highly tunable, e.g., via the modular organic bridges connect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90cffa67ab0531d8a8d8b6c8d090c069
https://doi.org/10.26434/chemrxiv-2023-gcwqn
https://doi.org/10.26434/chemrxiv-2023-gcwqn
A family of neutral cobalt complexes, [CpR'Co(Ropda)] 1-5, based on the redox-active o-phenylenediamide ligand (Ropda) undergo reversible 2e- oxidation revealed by cyclic voltammetry. This multielectron behavior is observed for all complexes regardle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7308c485c2aa892c29e3dca474272f70
https://doi.org/10.26434/chemrxiv-2023-l58hm
https://doi.org/10.26434/chemrxiv-2023-l58hm
Autor:
Santanu Malakar, Karsten Krogh-Jespersen, David Owen Marler, Alan S. Goldman, Xiaoguang Zhou, Thomas J. Emge, Wang Kun, Thomas Dugan, Aaron Sattler
Publikováno v:
ACS Catalysis. 11:14194-14209
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e2dd95537736b96f5e796e6bfccefe9
https://doi.org/10.1021/acscatal.1c03562
https://doi.org/10.1021/acscatal.1c03562
Autor:
Yue Sun, Thomas J. Emge, Yanbang Li, Josep M. Poblet, Mark C. Lipke, Iram F. Mansoor, Antonio Rodríguez-Fortea, William P. Kopcha, Gene S. Hall, Jianyuan Zhang, Antonio Moreno-Vicente
Publikováno v:
Angewandte Chemie. 133:25473-25477
New multicomponent reactions involving an isocyanide, terminal or internal alkynes, and endohedral metallofullerene (EMF) Lu3 N@C80 yield metallofulleroids which are characterized by mass-spectrometry, HPLC, and multiple 1D and 2D NMR techniques. Sin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e84dc3b61ccc6f43a70fc5c18f6c368b
https://doi.org/10.1002/ange.202110881
https://doi.org/10.1002/ange.202110881
Publikováno v:
Organic letters. 24(35)
The oxidative [4 + 2] reaction of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8bc30c1a925fea097653622b69bceaa
https://pubmed.ncbi.nlm.nih.gov/36036909
https://pubmed.ncbi.nlm.nih.gov/36036909
Autor:
Raheel Ahmad, Alexei M. Tyryshkin, Lingjun Xie, William A. Hansen, Brahm J. Yachnin, Thomas J. Emge, Ashraf Mashrai, Sagar D. Khare, Spencer Knapp
Publikováno v:
Journal of Inorganic Biochemistry. 244:112206
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d401d705c920cb4c824ea5b46407c1d
https://doi.org/10.1016/j.jinorgbio.2023.112206
https://doi.org/10.1016/j.jinorgbio.2023.112206
Publikováno v:
ACS Catalysis. 11:3009-3016
Dehydrogenation to give olefins offers the most broadly applicable route to the chemical transformation of alkanes. Transition-metal-based catalysts can selectively dehydrogenate alkanes using eith...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca916fa5905266a79490794c13db0249
https://doi.org/10.1021/acscatal.0c05160
https://doi.org/10.1021/acscatal.0c05160