Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Carl Thomas Bormann"'
Autor:
Farzaneh Fadaei-Tirani, Florian G. Abela, Rosario Scopelliti, Carl Thomas Bormann, Kay Severin
Publikováno v:
European Journal of Organic Chemistry. 2020:2130-2139
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e2d7ad4cf3b415e27eb03a8983c259d
https://doi.org/10.1002/ejoc.202000195
https://doi.org/10.1002/ejoc.202000195
Publikováno v:
ACS Catalysis. 10:3790-3796
Fluorinated pyridones are an important scaffold displaying relevant biological activities. Efficient assembly strategies of pyridones are transition metal-catalyzed C–H annulations with alkynes. The inaccessibility and extreme lability of fluoro al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c75689fa49606cec5931c814ea681468
https://doi.org/10.1021/acscatal.0c00499
https://doi.org/10.1021/acscatal.0c00499
Chemo- and regio-divergent access to fluorinated 1-alkyl and 1-acyl triazenes from alkynyl triazenes
Publikováno v:
Chemical science. 13(12)
The 1,1,2,2-tetrafluoroethylene unit is prevalent in bioactive molecules and functional materials. Despite being in principle a straightforward strategy to access this motif, the direct tetrafluorination of alkynes involves very hazardous or inconven
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db15fde9dc8bc14c907b6d2b88491970
https://pubmed.ncbi.nlm.nih.gov/35432853
https://pubmed.ncbi.nlm.nih.gov/35432853
Autor:
Florian Gérald Perrin, Nicolai Cramer, Carl Thomas Bormann, Jin-Fay Tan, F. Mark Chadwick, Kay Severin
Publikováno v:
Journal of the American Chemical Society. 141:10372-10383
Densely substituted fused aromatic triazenes can be prepared by [2 + 2 + 2] cyclotrimerization reactions of 1-alkynyl triazenes. The Cp*Ru-catalyzed cyclization proceeds well with both simple alkynyl triazenes and tethered 1-diynyl triazenes. Attract
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d571d454a87545366ddd324993ca1e0
https://doi.org/10.1021/jacs.9b04111
https://doi.org/10.1021/jacs.9b04111
Publikováno v:
Chemical Science
The 2-pyrone motif occurs frequently in bioactive natural products and is appreciated as synthetic intermediates. However, only few methods allow for diversifying functional group modifications on this relevant heterocycle. The distinct properties of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3efcffaee5889da32682bc6ba08a8e1
https://pubmed.ncbi.nlm.nih.gov/34276943
https://pubmed.ncbi.nlm.nih.gov/34276943
Cyclic olefins with triazene functions can display interesting reactivity, but synthetic access to these compounds is limited thus far. Herein, we describe the synthesis of cyclobutenyl triazenes fused to cyclopentanone or cyclohexanone rings. The bi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5b60293fc639f10e95eedf5fa2646eb
https://infoscience.epfl.ch/record/288446
https://infoscience.epfl.ch/record/288446
Autor:
Suleymanov, Abdusalom A.1 (AUTHOR), Severin, Kay1 (AUTHOR) kay.severin@epfl.ch
Publikováno v:
Angewandte Chemie. 3/22/2021, Vol. 133 Issue 13, p6955-6965. 11p.
Publikováno v:
Chemical Science; 3/28/2022, Vol. 13 Issue 12, p3305-3314, 10p
Publikováno v:
Chemical Science; 3/28/2022, Vol. 13 Issue 12, p3409-3415, 7p
Publikováno v:
Organic & Biomolecular Chemistry; 10/7/2021, Vol. 19 Issue 37, p7941-7948, 8p