101419-76-5Relevant articles and documents
A Facile Synthesis of 7-Halo-5H-indenopyridines and -pyridin-5-ones
DuPriest, Mark T.,Schmidt, Charles L.,Kuzmich, Daniel,Williams, Stanly B
, p. 2021 - 2023 (1986)
The 2-aryl-3-methylpyridines 7a-c were obtained in good yield by the addition of the corresponding aryllithium to 2-fluoro-3-methylpyridine.Permanganate oxidation provided the 2-aryl-3-pyridinecarboxylic acids 8a-c which were cyclized to 5H-indenopyridin-5-ones 6a-c in hot polyphosphoric acid.The 5H-indenopyridines 5a-c were readily obtained from the ketones 6a-c by treatment with hydrazine in hot diethylene glycol.
ORGANIC METAL COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE including same
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Paragraph 0072-0074, (2021/06/22)
Organic metal compounds, and organic light-emitting devices including the same are provided. The organic metal compound has a chemical structure of Formula (I):The definitions of R1-R18 and n are as defined in specification.
Scope of regioselective Suzuki reactions in the synthesis of arylpyridines and benzylpyridines and subsequent intramolecular cyclizations to azafluorenes and azafluorenones
Laha, Joydev K.,Patel, Ketul V.,Saima,Pandey, Surabhi,Solanke, Ganesh,Vashisht, Vanya
supporting information, p. 16069 - 16074 (2018/10/04)
The current investigation on regioselective Suzuki reactions of 2,3-dihalopyridines and 2-halo-3-halomethylpyridines yielded the unexplored synthesis of arylpyridines and benzylpyridines bearing synthetic handles for further functionalization. Indeed, the scope of intramolecular cyclizations of arylpyridines and benzylpyridines prepared in this study for the synthesis of azafluorenes and azafluorenones has been investigated.