Zobrazeno 1 - 10
of 122
pro vyhledávání: '"David Lebœuf"'
Publikováno v:
ACS Organic & Inorganic Au, Vol 4, Iss 3, Pp 287-300 (2024)
Externí odkaz:
https://doaj.org/article/abdaf8a5bd714692932e604781fd94ab
Autor:
Yuhao Ye, Akiyoshi Yamada, Yuto Kinoshita, Jinhua Wang, Pan Nie, Liangcai Xu, Huakun Zuo, Masashi Tokunaga, Neil Harrison, Ross D. McDonald, Alexey V. Suslov, Arzhang Ardavan, Moon-Sun Nam, David LeBoeuf, Cyril Proust, Benoît Fauqué, Yuki Fuseya, Zengwei Zhu, Kamran Behnia
Publikováno v:
npj Quantum Materials, Vol 9, Iss 1, Pp 1-9 (2024)
Abstract Bulk bismuth has a complex Landau spectrum. The small effective masses and the large g-factors are anisotropic. The chemical potential drifts at high magnetic fields. Moreover, twin boundaries further complexify the interpretation of the dat
Externí odkaz:
https://doaj.org/article/f2e92e7abc494ba48d59f41eb9ec543a
Autor:
Edoardo Martino, Carsten Putzke, Markus König, Philip J. W. Moll, Helmuth Berger, David LeBoeuf, Maxime Leroux, Cyril Proust, Ana Akrap, Holm Kirmse, Christoph Koch, ShengNan Zhang, QuanSheng Wu, Oleg V. Yazyev, László Forró, Konstantin Semeniuk
Publikováno v:
npj 2D Materials and Applications, Vol 5, Iss 1, Pp 1-7 (2021)
Abstract Crystalline defects can modify quantum interactions in solids, causing unintuitive, even favourable, properties such as quantum Hall effect or superconducting vortex pinning. Here we present another example of this notion—an unexpected uni
Externí odkaz:
https://doaj.org/article/7a4792590931431faf811c8ae43e628e
Autor:
Itai Keren, Tom Dvir, Ayelet Zalic, Amir Iluz, David LeBoeuf, Kenji Watanabe, Takashi Taniguchi, Hadar Steinberg
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-9 (2020)
Here, the authors develop a spectroscopic technique whereby individual defects in an ultrathin hBN dielectric, placed in proximity to graphene, act as quantum dots. Dot-assisted tunneling is highly sensitive to the nearby graphene excitation spectrum
Externí odkaz:
https://doaj.org/article/a91caf1dc4b945d990c3b931a83c7d5c
Publikováno v:
Chemical Communications. 59:6231-6234
A new class of self-assembled bidentate NDI-derived ligands featuring π–π interactions is described, which were successfully used in rhodium-catalyzed enantioselective hydrogenation of diverse olefins.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e90c6cd6700d1216dc382415972e157a
https://doi.org/10.1039/d3cc00695f
https://doi.org/10.1039/d3cc00695f
Publikováno v:
Chemical Science. 14:2983-2989
The use of epoxides as aldehyde surrogates allows isochromans to be constructed with greater scope than previously reported oxa-Pictet–Spengler reactions. The initial Meinwald rearrangement and subsequent steps are promoted by HFIP and triflic acid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::645a861860a98519b49adafc63100982
https://doi.org/10.1039/d2sc06692k
https://doi.org/10.1039/d2sc06692k
Publikováno v:
ACS Catalysis. 12:10995-11001
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a53f72f1ea1b0293699612c172fbffc
https://doi.org/10.1021/acscatal.2c03330
https://doi.org/10.1021/acscatal.2c03330
Publikováno v:
ACS Catalysis
ACS Catalysis, 2022, 12 (6), pp.3309-3316. ⟨10.1021/acscatal.2c00216⟩
ACS Catalysis, 2022, 12 (6), pp.3309-3316. ⟨10.1021/acscatal.2c00216⟩
The reduction of epoxides is a powerful tool to access anti-Markovnikov alcohols, but reported methods are poorly compatible with strongly electronically deactivated substrates. Here, we describe a general method for the linear-selective reduction of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c695299e5ba565f1af21189c5b683cf
https://doi.org/10.1021/acscatal.2c00216
https://doi.org/10.1021/acscatal.2c00216
Publikováno v:
Angewandte Chemie. 135
β-Arylethylamines are prevalent structural motifs in molecules exhibiting biological activity. Here we report a sequential one-pot protocol for the 1,2-aminoarylation of alkenes with hydroxylammonium triflate salts and (hetero)arenes. Unlike existin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ef2e78b4549f518e8ec7cce3b9833f1
https://doi.org/10.1002/ange.202215257
https://doi.org/10.1002/ange.202215257
Autor:
Tommaso Bortolato, Gianluca Simionato, Marie Vayer, Cristian Rosso, Lorenzo Paoloni, Edmondo M. Benetti, Andrea Sartorel, David Lebœuf, Luca Dell’Amico
Photocatalysis has become a prominent tool in the arsenal of organic chemists to develop and (re)imagine transformations. However, only a handful of versatile organic photocatalysts (PCs) are available, hampering the discovery of new reactivities. He
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e67f90c3da497e826a4adfb8366eda70
https://hdl.handle.net/11577/3466221
https://hdl.handle.net/11577/3466221
