Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Agnideep Das"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 858-870 (2020)
Copper catalysis finds applications in various synthetic fields by utilizing the ability of copper to sustain mono- and bielectronic elementary steps. Further to the development of well-defined copper complexes with classical ligands such as phosphin
Externí odkaz:
https://doaj.org/article/89b12727ee93421382934294fac4895a
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 858-870 (2020)
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 858-870 (2020)
Copper catalysis finds applications in various synthetic fields by utilizing the ability of copper to sustain mono- and bielectronic elementary steps. Further to the development of well-defined copper complexes with classical ligands such as phosphin
Publikováno v:
Chemical Society Reviews. 49:8840-8867
Biological systems provide attractive reactivity blueprints for the design of challenging chemical transformations. Emulating the operating mode of natural systems may however not be so easy and direct translation of structural observations does not
A hybrid bioinspired catechol-alloxazine triangular nickel complex stabilizing protons and electrons
Autor:
Stefani Gamboa-Ramirez, Guillaume Rogez, Zahia Boubegtiten-Fezoua, Agnideep Das, Aurélie Guenet, Laurence Grimaud, Maylis Orio, Marine Desage-El Murr, Sylvie Choua, Hannah Jobelius, Petra Hellwig, Jésus Raya, Jules Schleinitz, Geordie Creste, Gwendal Kervern, Sylvie Ferlay, Nolwenn Le Breton
We report the design of a unique bioinspired ligand merging redox-active catechol and flavin-related alloxazine substructures. Upon coordination with a Ni(II) salt, this hybrid ligand forms a trinuclear complex containing three NiII centers and three
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb2a90b135b13e8a7fc76048e7cfb92e
http://xlink.rsc.org/?DOI=D1QI01131F
http://xlink.rsc.org/?DOI=D1QI01131F
Autor:
S. Yamago, G. M. Sammis, Davide Ravelli, M. Fagnoni, M. P. Sibi, Cheriehan Hessin, S. Protti, K. Mitsudo, H. Subramaniann, J. A. Murphy, Yufeng Ren, D. Dimitrova, Louis Fensterbank, R. A. Ii Flowers, A. Pérez-Luna, Cyril Ollivier, I. Ryu, T. G. Bolduc, J.-P. Goddard, S. Sumino, M. Desage-El Murr, T. Qin, B. Thomson, K. F. Clark, M. Zhou, Y. Lu, T. Fukuyama, Agnideep Das, S. Suga, Fabrice Chemla, M. Cormier, Caroline O. Bartulovich, Z.-Q. Liu, Tesia V. Chciuk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb09eb2f4a7182414545464832dbfadc
https://doi.org/10.1055/b000000086
https://doi.org/10.1055/b000000086
Publikováno v:
Free Radicals: Fundamentals and Applications in Organic Synthesis 2
Redox-active ligands are well known for their ability to stabilize electronic density on their scaffolds, and coordination complexes with such ligands are often stable, open-shell species. This property can be used as a means to favor single-electron
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b73ce04c8e2274358e45023383aa208e
https://doi.org/10.1055/sos-sd-233-00066
https://doi.org/10.1055/sos-sd-233-00066