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C-H Imidation of 7-Deazapurines
- 1.0491246 - ÚOCHB 2019 RIV US eng J - Journal Article
Sabat, Nazarii - Poštová Slavětínská, Lenka - Klepetářová, Blanka - Hocek, Michal
C-H Imidation of 7-Deazapurines.
ACS Omega. Roč. 3, č. 4 (2018), s. 4674-4678. ISSN 2470-1343. E-ISSN 2470-1343
R&D Projects: GA ČR(CZ) GA16-00178S; GA MŠMT(CZ) LO1304
Grant - others:AV ČR(CZ) AP1501
Program: Akademická prémie - Praemium Academiae
Institutional support: RVO:61388963
Keywords : cross-coupling reactions * pyrimidine nucleosides * bond functionalization
OECD category: Organic chemistry
Impact factor: 2.584, year: 2018
https://pubs.acs.org/doi/10.1021/acsomega.8b00520
We developed and presented here a ferrocene-catalyzed C-H imidation of 7-deazapurines (pyrrolo[2,3-d]pyrimidines) with N-imidyl peroxyesters. The reactions occur regioselectively at position 8 in 7-deazapurines, leading to a series of 8-succinimido-, phtalimido-, or naphthalimido-7-deazapurine derivatives. Attempted hydrazinolysis of resulting 8-imidyl-7-deazapurines led to corresponding 8-amino-7-deazapurine, which was very unstable and quickly decomposed.
Permanent Link: http://hdl.handle.net/11104/0285280
Number of the records: 1