Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Dmitry Dibchak"'
Autor:
Dmitry Dibchak, Mariya Snisarenko, Artem Mishuk, Oleg Shablykin, Lina Bortnichuk, Oleksii Klymenko-Ulianov, Yurii Kheylik, Iryna Sadkova, Henry Rzepa, Pavel Mykhailiuk
A general approach to 3-azabicyclo[3.1.1]heptanes was unexpectedly discovered. The mechanism, scope, and scalability of this method were studied. The core was incorporated into the structure of the antihistamine drug Rupatidine instead of the pyridin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7e427db48da5435aa4ebec9aa25792a
https://doi.org/10.26434/chemrxiv-2023-jbb0r
https://doi.org/10.26434/chemrxiv-2023-jbb0r
Autor:
Valeriya Shcherbakova, Pavel K. Mykhailiuk, Yevhen Skalenko, Dmitry Dibchak, Mariya Snisarenko, Aleksandr V. Denisenko, Anastasiia S. Kuznetsova
Publikováno v:
The Journal of Organic Chemistry. 86:2200-2209
A synthetic strategy to fused bicyclic piperidines-building blocks for medicinal chemistry-is developed. The key step was an intramolecular [2 + 2]-photocyclization. The photochemical step was performed on a gram scale. Crystallographic analysis of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e3a1efc810431aab90ac328511dcdc3
https://doi.org/10.1021/acs.joc.0c02355
https://doi.org/10.1021/acs.joc.0c02355
Autor:
Valeriya, Shcherbakova, Dmitry, Dibchak, Mariya, Snisarenko, Yevhen, Skalenko, Aleksandr V, Denisenko, Anastasiia S, Kuznetsova, Pavel K, Mykhailiuk
Publikováno v:
The Journal of organic chemistry. 86(3)
A synthetic strategy to fused bicyclic piperidines-building blocks for medicinal chemistry-is developed. The key step was an intramolecular [2 + 2]-photocyclization. The photochemical step was performed on a gram scale. Crystallographic analysis of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5094c7e89db5be19889ed5f3c7731b9d
https://pubmed.ncbi.nlm.nih.gov/33211487
https://pubmed.ncbi.nlm.nih.gov/33211487
Publikováno v:
Organic letters. 21(22)
Synthesis of the previously unknown conformationally rigid sultams fused with the cyclobutane ring was developed. The key transformation was an intramolecular photochemical cyclization of linear sulfonamides. Crystallographic analysis showed that the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da231b4c35cabf36f5ca794072c8db25
https://pubmed.ncbi.nlm.nih.gov/31603689
https://pubmed.ncbi.nlm.nih.gov/31603689