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pro vyhledávání: '"Carbene compounds"'
Akademický článek
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Autor:
Brusar, Vedran, Forjan, Mateo, Ljubić, Ivan, Alešković, Marija, Becker, Kristin, Vdović, Silvije
Publikováno v:
The Journal of Organic Chemistry. 88:4286-4300
The photochemical reactivity of diphenyldiazomethane 1 and phenyl 1- and 2 adamantyl diazomethanes 2 and 3, respectively, was investigated by transient absorption spectroscopy (TA). Photoelimination of N2 upon UV excitation takes place in the anti-Ka
Autor:
Rossana Galassi, Lorenzo Luciani, Junbiao Wang, Silvia Vincenzetti, Lishan Cui, Augusto Amici, Stefania Pucciarelli, Cristina Marchini
Publikováno v:
Biomolecules, Vol 12, Iss 1, p 80 (2022)
Breast cancers (BCs) may present dramatic diagnoses, both for ineffective therapies and for the limited outcomes in terms of lifespan. For these types of tumors, the search for new drugs is a primary necessity. It is widely recognized that gold compo
Externí odkaz:
https://doaj.org/article/7da8a46bb4064ab99d63ef0bbf219080
Publikováno v:
Organometallics
Organometallics, 2022, 41 (20), pp.2868-2878. ⟨10.1021/acs.organomet.2c00429⟩
Organometallics, 2022, 41 (20), pp.2868-2878. ⟨10.1021/acs.organomet.2c00429⟩
International audience; Thanks to the onio-substitution strategy, tricationic imidazolium salt (1·H)(OTf)3 featuring two N-cyclopropenio substituents was readily prepared in a two-step procedure from 1H-imidazole. The influence of the two cycloprope
Autor:
Pizarro Javier, Juan Diego, Schmidtke, Inga L., Nova, Ainara, Romero Fructos-Vázquez, Manuel, Pérez Romero, Pedro José
Publikováno v:
ACS Catalysis. 12:6851-6856
The complete regioselective incorporation of carbene units to nonactivated arene rings has been achieved employing gold(I) catalysts bearing alkoxydiaminophosphine ligands, with readily available, nonelaborated ethyl 2-phenyl-diazoacetate as the carb
Publikováno v:
Journal of the American Chemical Society. 144(51)
Control of the regioselectivity in the functionalization of C–H bonds of linear alkanes C2H2n+2 via carbene transfer from diazo compounds is restricted to the use of rhodium-based catalysts, which govern the reaction outcome employing donor–accep
Autor:
Cintia Virumbrales, Mahmoud A. E. A. A. A. El-Remaily, Samuel Suárez-Pantiga, Manuel A. Fernández-Rodríguez, Félix Rodríguez, Roberto Sanz
Publikováno v:
Scopus
A gold(I)-catalyzed cascade reaction for the stereoselective synthesis of sulfur- or selenium-containing indeno[1,2-b]chromene derivatives from o-(alkynyl)styrenes substituted at the triple bond with a thio- or seleno-aryl group is described. The rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85d1fa5fdb6bacafbb03a85b8a46505c
http://hdl.handle.net/10259/7405
http://hdl.handle.net/10259/7405
Autor:
Rubén M. Carballo, José M. Padrón, Israel Fernández, Daniel A. Cruz, Luana Grmuša, Víctor S. Martín, Juan I. Padrón
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
A direct, catalytic, and complementary method to obtain 2-substituted homoallyl sulfonyl amides is described, starting from sulfonyl amides, aldehydes, and allyltrimethylsilane using iron(III) chloride as a sustainable catalyst. The scope of the proc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d2238140e8f885cc8cfca001e9f6320
http://hdl.handle.net/10261/278954
http://hdl.handle.net/10261/278954
Autor:
Haritz Sardon, Ricardo A. Pérez-Camargo, Ying Zhao, Guoming Liu, Leire Meabe, Alejandro J. Müller, Dujin Wang
Publikováno v:
Macromolecules. 54:7258-7268
Unformatted post-print version of the accepted article Poly (hexamethylene carbonate) (PC6) and poly (octamethylene carbonate) (PC8) were studied under different crystallization conditions. Using differential scanning calorimetry (DSC), a new solid-s
Autor:
Murray G. Rosenberg, Udo H. Brinker
The abstract is available here: https://uscholar.univie.ac.at/o:1637057
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::989450c1aa60c7c8e2d9ffdaee1d3b4a
https://phaidra.univie.ac.at/o:1637057
https://phaidra.univie.ac.at/o:1637057