Zobrazeno 1 - 10
of 604
pro vyhledávání: '"G, Kokotos"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 20, Iss 1, Pp 379-426 (2024)
The synthesis of indoles and their derivatives, more specifically bis(indolyl)methanes (BIMs), has been an area of great interest in organic chemistry, since these compounds exhibit a range of interesting biological and pharmacological properties. BI
Externí odkaz:
https://doaj.org/article/5d55cea056024ab4a266f075cc604c7d
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 833-857 (2020)
Photochemistry, the use of light to promote organic transformations, has been known for more than a century but only recently has revolutionized the way modern chemists are thinking. Except from transition metal-based complexes, small organic molecul
Externí odkaz:
https://doaj.org/article/072272432dd54f878403d7d420404d25
Publikováno v:
Homologation Reactions. :309-351
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c009690a3ba0608ab394d591fb7f860
https://doi.org/10.1002/9783527830237.ch8
https://doi.org/10.1002/9783527830237.ch8
Publikováno v:
Trends in Chemistry. 5:116-120
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b07594bcdd610219a589eb693805404
https://doi.org/10.1016/j.trechm.2022.10.003
https://doi.org/10.1016/j.trechm.2022.10.003
Autor:
Naya A. Stini, Efthymios T. Poursaitidis, Nikolaos F. Nikitas, Michail Kartsinis, Nikoleta Spiliopoulou, Phoebe Ananida-Dasenaki, Christoforos G. Kokotos
Publikováno v:
Organic & Biomolecular Chemistry. 21:1284-1293
A light-promoted hydroacylation of dialkyl azodicarboxylates in moderate to high yields (52–97%) and short reaction times (15–210 min) is described. Application of the reaction in the synthesis of Moclobemide and Vorinostat is demonstrated.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0fb9aba9ec2ad419bb5af702913c500
https://doi.org/10.1039/d2ob02204d
https://doi.org/10.1039/d2ob02204d
Autor:
Eirini M. Galathri, Lorenzo Di Terlizzi, Maurizio Fagnoni, Stefano Protti, Christoforos G. Kokotos
Publikováno v:
Organic & Biomolecular Chemistry. 21:365-369
A mild, low-cost and green protocol for the photochemical Friedel–Crafts arylation of aldehydes with indoles, utilizing arylazo sulfones as the photoacid generator.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b23a33ba3c39e1e3d1214fd202696fdd
https://doi.org/10.1039/d2ob02214a
https://doi.org/10.1039/d2ob02214a
Autor:
Elpida Skolia, Christoforos G. Kokotos
Publikováno v:
ACS Organic & Inorganic Au. 3:96-103
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5899015a2526cd686193d9a6bf64077c
https://doi.org/10.1021/acsorginorgau.2c00053
https://doi.org/10.1021/acsorginorgau.2c00053
Autor:
Constantinos T. Constantinou, Petros L. Gkizis, Olga Thomais G. Lagopanagiotopoulou, Elpida Skolia, Nikolaos F. Nikitas, Ierasia Triandafillidi, Christoforos G. Kokotos
Publikováno v:
Chemistry – A European Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d911a43cb6cf38112341794db30ed3e
https://doi.org/10.1002/chem.202301268
https://doi.org/10.1002/chem.202301268
Autor:
Olga G. Mountanea, Danai Psathopoulou, Christiana Mantzourani, Maroula G. Kokotou, E. Alexandros Routsi, Demeter Tzeli, Christoforos G. Kokotos, George Kokotos
Publikováno v:
Chemistry – A European Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e4a8f52bfb84dd7af2a7f0d23bf1cc9
https://doi.org/10.1002/chem.202300556
https://doi.org/10.1002/chem.202300556
Autor:
Christoforos G. Kokotos, Angelos Balaskas, Stamatis K. Serviou, Petros L. Gkizis, Constantinos T. Constantinou, Ierasia Triandafillidi
Publikováno v:
Synlett.
The phenol moiety appears in a wide variety of natural products, exhibiting biological activity, and in numerous active pharmaceutical compounds. Boronic acids are potential precursors of the phenol scaffold, and a plethora of efforts has been focuse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a04e3365f01d3f09fc8720d4b840e9d
https://doi.org/10.1055/a-2071-7077
https://doi.org/10.1055/a-2071-7077