Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Philipp Spieß"'
Publikováno v:
Accounts of Chemical Research.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bdcfcd52d5007a16c25177d3c1799409
https://doi.org/10.1021/acs.accounts.3c00171
https://doi.org/10.1021/acs.accounts.3c00171
Publikováno v:
Organic Letters. 23:4179-4184
An alternative and complementary transformation for the synthesis of aryl- and heteroaryl-substituted alkynes is presented that relies on a chemoselective electrocoupling process. Tetraorganoborate substrates were logically designed and simply access
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7076c62c65ae7bd45da825107536977
https://doi.org/10.1021/acs.orglett.1c01126
https://doi.org/10.1021/acs.orglett.1c01126
Autor:
Philipp Spieß, Konstantin Karaghiosoff, Paul Knochel, Lucie Grokenberger, Jeffrey M. Hammann, Ferdinand H. Lutter
Publikováno v:
Angewandte Chemie (International Ed. in English)
A combination of 10 % CoCl2 and 20 % 2,2′‐bipyridine ligands enables cross‐coupling of functionalized primary and secondary alkylzinc reagents with various (hetero)aryl halides. Couplings with 1,3‐ and 1,4‐substituted cycloalkylzinc reagent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7c3923caf9002c443b4de30f0e1d582
https://doi.org/10.1002/anie.201914490
https://doi.org/10.1002/anie.201914490
Autor:
Philipp Spieß, Lucie Grokenberger, Paul Knochel, Ferdinand H. Lutter, Konstantin Karaghiosoff, Jeffrey M. Hammann
Publikováno v:
Angewandte Chemie. 132:5591-5595
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ab01d2fca20d11301b439c7ccca895f
https://doi.org/10.1002/ange.201914490
https://doi.org/10.1002/ange.201914490
Publikováno v:
Journal of the American Chemical Society
A novel, one-step N-dehydrogenation of amides to enamides is reported. This reaction employs the unlikely combination of LiHMDS and triflic anhydride, which serves as both the electrophilic activator and the oxidant, and is characterized by its simpl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3e5225583a73012d9d8e6aa662171f4
https://pubmed.ncbi.nlm.nih.gov/34232035
https://pubmed.ncbi.nlm.nih.gov/34232035
Publikováno v:
Organic letters. 23(11)
An alternative and complementary transformation for the synthesis of aryl- and heteroaryl-substituted alkynes is presented that relies on a chemoselective electrocoupling process. Tetraorganoborate substrates were logically designed and simply access
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9eef9d03d04e657061c2bdacda266cb4
https://pubmed.ncbi.nlm.nih.gov/34004116
https://pubmed.ncbi.nlm.nih.gov/34004116
Publikováno v:
Angewandte Chemie (International ed. in English). 60(21)
A catalytic 1,1-difunctionalization of unactivated olefins en route to sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b88f7ea7122458b9462f5812a87c1612
https://pubmed.ncbi.nlm.nih.gov/33630396
https://pubmed.ncbi.nlm.nih.gov/33630396
Autor:
Dorian Didier, Philipp Spieß, Andreas N. Baumann, Thomas-C. Jagau, Arif Music, Allan Plantefol
We report herein versatile, transition metal-free and additive-free (hetero)aryl-aryl coupling reactions promoted by the oxidative electrocoupling of unsymmetrical tetra(hetero)arylborates (TABs) prepared from ligand-exchange reactions on potassium t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21a0d206bd4cbe38e5f3ed49f3b41620
https://lirias.kuleuven.be/handle/123456789/654194
https://lirias.kuleuven.be/handle/123456789/654194
Autor:
Jörg Stierstorfer, Norbert Szimhardt, Philipp Spieß, Maximilian H. H. Wurzenberger, Thomas M. Klapötke
Publikováno v:
Propellants, Explosives, Pyrotechnics. 43:1203-1209
Since the nowadays used lead-based primary explosives, lead azide, picrate and styphnate suffer from various environmental and toxic issues, there is a great need for new green materials. Therefore, two highly promising lead-free primary explosives p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a57ab230823248b1ac11114be5e854a
https://doi.org/10.1002/prep.201800221
https://doi.org/10.1002/prep.201800221