Zobrazeno 1 - 10
of 323
pro vyhledávání: '"M. Amberg"'
Autor:
C. Landelle, J. Caron-Guyon, B. Nazarian, J.L. Anton, J. Sein, L. Pruvost, M. Amberg, F. Giraud, O. Félician, J. Danna, A. Kavounoudias
Publikováno v:
iScience, Vol 26, Iss 10, Pp 107965- (2023)
Summary: Texture, a fundamental object attribute, is perceived through multisensory information including touch and auditory cues. Coherent perceptions may rely on shared texture representations across different senses in the brain. To test this hypo
Externí odkaz:
https://doaj.org/article/8a7f69bbd0754899a318d6e970529079
Autor:
C. Landelle, J. Danna, B. Nazarian, M. Amberg, F. Giraud, L. Pruvost, R. Kronland-Martinet, S. Ystad, M. Aramaki, Anne Kavounoudias
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Abstract Combining multisensory sources is crucial to interact with our environment, especially for older people who are facing sensory declines. Here, we examined the influence of textured sounds on haptic exploration of artificial textures in healt
Externí odkaz:
https://doaj.org/article/00a835e9bc18484cb9789e5e7bca59e3
Publikováno v:
Physical Review Special Topics. Accelerators and Beams, Vol 13, Iss 4, p 041302 (2010)
The crossbar-H-mode (CH) structure is the first superconducting multicell drift tube cavity for the low and medium energy range operated in the H_{21} mode. Because of the large energy gain per cavity, which leads to high real estate gradients, it is
Externí odkaz:
https://doaj.org/article/3c47b0866593459399323c123cfd7ba2
Publikováno v:
Journal of the American Chemical Society. 145:774-780
Intermolecular cyclopropanation of mono-, di-, and trisubstituted olefins with α-bromo-β-ketoesters and α-bromomalonates under organophotocatalysis is reported. The reaction displays broad functional group tolerance, including substrates bearing a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3688f70b07b371c0bbc5f76ec25b9743
https://doi.org/10.1021/jacs.2c11680
https://doi.org/10.1021/jacs.2c11680
Autor:
Erick Carreira, Willi M. Amberg
Publikováno v:
Journal of the American Chemical Society. 144:15475-15479
We disclose the first total synthesis of (+)-aberrarone, a diterpenoid natural product featuring a 5-5-5-6-fused tetracyclic skeleton. Key to the approach is a Au-catalyzed-Sn-mediated Meyer-Schuster-Nazarov-cyclopropanation-aldol cascade, which clos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::083e3a1c315fceef6775686af56ea297
https://doi.org/10.1021/jacs.2c07150
https://doi.org/10.1021/jacs.2c07150
Autor:
Willi M. Amberg, Sebastian N. Intorp, Evgenia Dmitrieva, Alexey A. Popov, Frank Rominger, Jan Freudenberg, Uwe H. F. Bunz
Publikováno v:
Chemistry – A European Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79ea8ff8cc2c5119db973123a9ea52c5
https://doi.org/10.1002/chem.202203862
https://doi.org/10.1002/chem.202203862
Autor:
Sean M. Amberg, Benjamin Snyder, Portia A. Vliet-Gregg, Eric J. Tarcha, Jeff Posakony, Kristin M. Bedard, Alison E. Heald
Publikováno v:
Antimicrobial Agents and Chemotherapy. 66
LHF-535 is a small-molecule antiviral currently under development as a therapeutic option to treat Lassa fever and other viral hemorrhagic fevers of arenavirus origin. The human safety and pharmacokinetics of LHF-535 were evaluated in two phase 1 tri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ee70a7e7dc7162fe40f9eee48141621
https://doi.org/10.1128/aac.00951-22
https://doi.org/10.1128/aac.00951-22
Publikováno v:
Journal of the American Chemical Society. 143:8261-8265
We disclose the first total synthesis of (+)-euphorikanin A, an ingenane-derived natural product featuring an unprecedented 5/6/7/3-fused tetracyclic skeleton. Key to the approach is a SmI2-mediated ketyl-enoate reaction that leads to the formation o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b51eef4bed618dabf09dbdb13e7eb106
https://doi.org/10.1021/jacs.1c04210
https://doi.org/10.1021/jacs.1c04210
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