Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Dorian Didier"'
Publikováno v:
Communications Chemistry, Vol 7, Iss 1, Pp 1-9 (2024)
Abstract Radical-polar crossover of organoborates is a poweful tool that enables the creation of two C-C bonds simultaneously. Small ring systems have become essential motifs in drug discovery and medicinal chemistry. However, step-economic methods f
Externí odkaz:
https://doaj.org/article/908724c52e7a4556af7fb5d34f7a7d08
Publikováno v:
Electrochemical Science Advances, Vol 2, Iss 1, Pp n/a-n/a (2022)
Abstract Cross‐coupling reactions for C–C bond formation represent a cornerstone of organic synthesis. In most cases, they make use of transition metals, which has several downsides. Recently, metal‐free alternatives relying on electrochemistry
Externí odkaz:
https://doaj.org/article/27dc64a14654483095a9388c0475e074
Autor:
Dorian Didier
Publikováno v:
Synthesis. 55:232-239
C–C bond formation has challenged the community of synthetic organic chemists for decades. Organoboron derivatives represent a mild and functional-group-tolerant class of reagents that can be handled without the need for inert conditions, making th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8370c08d460dc3784c810597a65a75eb
https://doi.org/10.1055/a-1757-2680
https://doi.org/10.1055/a-1757-2680
Publikováno v:
Nachrichten aus der Chemie. 69:72-75
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58def74e8df4e05a4bf0151653ec3eb6
https://doi.org/10.1002/nadc.20214119230
https://doi.org/10.1002/nadc.20214119230
Autor:
Felix Reiners, Dorian Didier
Publikováno v:
Nachrichten aus der Chemie. 69:70-74
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d4cb6e1508517d8d9839a61604fdc5a
https://doi.org/10.1002/nadc.20214112348
https://doi.org/10.1002/nadc.20214112348
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:
Felix Reiners, Dorian Didier
Publikováno v:
The Chemical Record. 21:1144-1160
Strained ring systems have gained considerable importance over the last few years for their implication in natural product syntheses or in drug discovery programs. We present herein a recollection of our work on the construction and functionalization
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::385eac50bcb0b1308e4434675279c3f0
https://doi.org/10.1002/tcr.202100011
https://doi.org/10.1002/tcr.202100011
Autor:
Felix Reiners, Dorian Didier
Publikováno v:
Nachrichten aus der Chemie. 69:72-75
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::469ba9daf056f006e72723715b3d4dec
https://doi.org/10.1002/nadc.20214106650
https://doi.org/10.1002/nadc.20214106650
Autor:
Thomas-C. Jagau, Arif Music, Florian Boser, Dorian Didier, Florian Matz, Andreas N. Baumann, Nicolas Müller
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
Readily accessible tetraorganoborate salts undergo selective coupling reactions under blue light irradiation in the presence of catalytic amounts of transition‐metal‐free acridinium photocatalysts to furnish unsymmetrical biaryls, heterobiaryls a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94f79f0e91095ed87df8de9500e2b633
https://doi.org/10.1002/chem.202005282
https://doi.org/10.1002/chem.202005282
Publikováno v:
Organic Letters. 22:8533-8537
Non-natural azetidine-based amino acids (Aze) present interesting features in protein engineering. A simple organometallic route toward unsaturated carboxylic acid precursors is presented. Subsequent metal-catalyzed asymmetric reduction allowed for t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::854622c0e5b2ddca81720e0775f4b4fe
https://doi.org/10.1021/acs.orglett.0c03131
https://doi.org/10.1021/acs.orglett.0c03131