Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Alexandra E. Bosnidou"'
Autor:
Viktoria A. Ikonnikova, Cristina Cheibas, Oscar Gayraud, Alexandra E. Bosnidou, Nicolas Casaretto, Gilles Frison, Bastien Nay
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 20, Iss 1, Pp 162-169 (2024)
The Hock cleavage, which is compatible with tandem processes, was applied to the synthesis of 1-aryltetralines through a one-pot transformation from readily available benzyl(prenyl)malonate substrates. After the photooxygenation of the prenyl moiety,
Externí odkaz:
https://doaj.org/article/90cd36c8172a4e9a82beed3902be4a6c
Publikováno v:
Iodine Catalysis in Organic Synthesis. :121-149
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46e3168b77fbae8cbfd2bc41a9f8d716
https://doi.org/10.1002/9783527829569.ch5
https://doi.org/10.1002/9783527829569.ch5
Autor:
Alexandra E. Bosnidou, Kilian Muñiz
Publikováno v:
Angewandte Chemie International Edition. 58:7485-7489
The direct amination of aliphatic C-H bonds has remained one of the most tantalizing transformations in organic chemistry. Herein, we report on a unique catalyst system, which enables the elusive intermolecular C(sp3 )-H amination. This practical syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::626e09aaa6768ed0d66ece1ae78a3aa1
https://doi.org/10.1002/anie.201901673
https://doi.org/10.1002/anie.201901673
Publikováno v:
European Journal of Organic Chemistry. 2020:6361-6365
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4bf18247227d78ecf5da129488a61cb
https://doi.org/10.1002/ejoc.201900497
https://doi.org/10.1002/ejoc.201900497
Autor:
Alexandra E. Bosnidou, Kilian Muñiz
Publikováno v:
Angewandte Chemie. 131:7564-7568
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df791abbd67263f52571103dd3bd334f
https://doi.org/10.1002/ange.201901673
https://doi.org/10.1002/ange.201901673
Publikováno v:
European Journal of Organic Chemistry. 2020:6368-6369
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8d45a98b36fb8f52bf9283a8f65434b
https://doi.org/10.1002/ejoc.202001088
https://doi.org/10.1002/ejoc.202001088
Autor:
Alexandra E. Bosnidou, Kilian Muñiz
Publikováno v:
Chemistry – A European Journal. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40577e091b1284b80af51d872f1745c4
https://doi.org/10.1002/chem.201986061
https://doi.org/10.1002/chem.201986061
Autor:
Kilian Muñiz, Alexandra E. Bosnidou
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 25(60)
In contrast to aryliodine(III) compounds, which have matured into a particularly attractive class of oxidants in modern synthesis, the synthetic potential of related alkyliodine(III) derivatives has remained widely underestimated. This is surprising
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f8647bf992a2af5e812ee5474ffe621
https://pubmed.ncbi.nlm.nih.gov/31361354
https://pubmed.ncbi.nlm.nih.gov/31361354
Autor:
Alexandra E, Bosnidou, Kilian, Muñiz
Publikováno v:
Angewandte Chemie (International ed. in English). 58(22)
The direct amination of aliphatic C-H bonds has remained one of the most tantalizing transformations in organic chemistry. Herein, we report on a unique catalyst system, which enables the elusive intermolecular C(sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8026b42f5500a97201ed8ceeeabd6b1a
https://pubmed.ncbi.nlm.nih.gov/30888107
https://pubmed.ncbi.nlm.nih.gov/30888107
Publikováno v:
Chemistry - A European Journal. 22:9929-9932
A photochemical catalytic amination of arenes is presented. The reaction proceeds under benign iodine catalysis in the presence of visible light as the initiator and provides access to a range of differently substituted arylamines. A total of 29 exam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::343ac11ad033ef5ffa8d8198cdd3993d
https://doi.org/10.1002/chem.201602138
https://doi.org/10.1002/chem.201602138