Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Pavel Fedoseev"'
Autor:
Gerardo M. Ojeda, Prabhat Ranjan, Pavel Fedoseev, Lisandra Amable, Upendra K. Sharma, Daniel G. Rivera, Erik V. Van der Eycken
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 2447-2457 (2019)
An efficient sequence based on the Ugi-azide reaction and rhodium(III)-catalyzed intermolecular annulation has been established for the preparation of tetrazole-isoquinolone/pyridone hybrids. Several N-acylaminomethyltetrazoles were reacted with aryl
Externí odkaz:
https://doaj.org/article/9a41587abdf84df8b78b9684defcd164
Autor:
Pavel Fedoseev
Publikováno v:
Образование и педагогическая наука в XXI веке: теоретические и практические аспекты исследований. Сборник статей III Всероссийской межвузовской научно-практической конференции.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17e10a8b2a56d5a3a4a32e5720036865
https://doi.org/10.52376/978-5-907419-23-0_273
https://doi.org/10.52376/978-5-907419-23-0_273
Autor:
Markus Furegati, Suzanna Clark, Andreas Marzinzik, Nikolaos Drosos, Emilie Joly, Patrick Schindler, Kristine Venstrom, Yannick Mesrouze, Yoko Oei, Marion Lacaud-Baumlin, Robert Martin Grotzfeld, Lionel Doumampouom-Metoul, Darryl Brynley Jones, Brian Granda, Sandro Nocito, Stephanie Lagasse-Guerro, Etienne Richard, Peiyin Wang, Sylvie Chamoin, Patrick J Rudewicz, Grazia Piizzi, Edwige Beng-Louka, Michael Patrick Dillon, Pavel Fedoseev, Alexei S. Karpov, Isabelle Dacquignies, Patrick Chène, Piotr Martyniuk, Francesca Perruccio, Cristina Nieto-Oberhuber, Marc Lafrance, Enrique Blanco, Mauro Zurini, Edward Lorenzana, William Mallet, Dylan Daniel, Tinya Abrams, Mélanie Velay
Publikováno v:
ACS Med Chem Lett
[Image: see text] Targeted antimitotic agents are a promising class of anticancer therapies. Herein, we describe the development of a potent and selective antimitotic Eg5 inhibitor based antibody–drug conjugate (ADC). Preliminary studies were perfo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4f60061fe25e069e99abe4fe52a72ca
https://europepmc.org/articles/PMC6912867/
https://europepmc.org/articles/PMC6912867/
Autor:
Prabhat Ranjan, Gerardo M. Ojeda, Lisandra Amable, Pavel Fedoseev, Erik V. Van der Eycken, Daniel G. Rivera, Upendra K. Sharma
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 2447-2457 (2019)
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 2447-2457 (2019)
An efficient sequence based on the Ugi-azide reaction and rhodium(III)-catalyzed intermolecular annulation has been established for the preparation of tetrazole-isoquinolone/pyridone hybrids. Several N-acylaminomethyltetrazoles were reacted with aryl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7015222ddf6923ef684246b80253d170
https://lirias.kuleuven.be/handle/123456789/642539
https://lirias.kuleuven.be/handle/123456789/642539
Publikováno v:
RSC Advances. 6:75202-75206
A diversity-oriented approach for the synthesis of 2-aminoimidazoles is presented. The method involves the cyclization of secondary propargylamines using iodine allowing the generation of diversely-substituted 2-aminoimidazoles. The iodo group genera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a55e2f99db4ae405d12e8fda63f459c7
https://doi.org/10.1039/c6ra13371a
https://doi.org/10.1039/c6ra13371a
A high-yielding fast spirocyclization of easily available indol ynones has been developed by applying N-iodosuccinimide. The formation of the desired product occurs in an atom-economical way, under mild conditions, instantly after the addition of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae22983fc2df998094cd43d4457a2870
https://lirias.kuleuven.be/handle/123456789/619815
https://lirias.kuleuven.be/handle/123456789/619815
Autor:
Erik V. Van der Eycken, Pavel Fedoseev
Publikováno v:
Chemical communications (Cambridge, England). 53(55)
A high-yielding, temperature switchable divergent approach towards the synthesis of either spiro-indolenines or quinolines is described, starting from easily available indolyl ynones. The application of TFA at rt promotes the dearomatization of the i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67f15788bce1ee5e63498de57f8d9d8b
https://pubmed.ncbi.nlm.nih.gov/28492644
https://pubmed.ncbi.nlm.nih.gov/28492644