Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Jeremy N. Ridenour"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 1933-1941 (2014)
Dimethyl (β-substituted) vinylphosphonates do not readily undergo cross metathesis reactions with Grubbs catalyst and terminal alkenes. However, the corresponding mono- or diallyl vinylphosphonate esters undergo facile cross metathesis reactions. Th
Externí odkaz:
https://doaj.org/article/7ab439c2dae040d8ba79626792c250fa
Publikováno v:
Organic letters. 22(10)
Nickel-catalyzed reductive addition of phosphonodienes to aldehydes (the Mori-Tamaru reaction) gives hydroxy vinyl phosphonates in good yields with excellent control of the relative stereochemistry. Base-induced cyclization of the vinyl phosphonates
Autor:
Laurent Kremer, Christopher D. Spilling, Jeremy N. Ridenour, Jean-Louis Herrmann, Vincent Le Moigne, Abdeldjalil Madani, Anosha Abdul Basir, Stéphane Audebert, Luc Camoin, Jean-François Cavalier, Stéphane Canaan, Benjamin P. Martin, Rishi R. Paudel
Publikováno v:
ACS Infectious Diseases
ACS Infectious Diseases, American Chemical Society, 2019, ⟨10.1021/acsinfecdis.9b00172⟩
ACS Infectious Diseases, 2019, ⟨10.1021/acsinfecdis.9b00172⟩
ACS Infectious Diseases, American Chemical Society, 2019, ⟨10.1021/acsinfecdis.9b00172⟩
ACS Infectious Diseases, 2019, ⟨10.1021/acsinfecdis.9b00172⟩
Twelve new Cyclophostin and Cyclipostins analogues (CyC19-30) were synthesized, thus extending our series to 38 CyCs. Their antibacterial activities were evaluated against four pathogenic mycobacteria (Mycobacterium abscessus, Mycobacterium marinum,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca422e4fbef357b2f8f85b979668191c
https://hal-amu.archives-ouvertes.fr/hal-02276160
https://hal-amu.archives-ouvertes.fr/hal-02276160