Name: 3-Pyridinecarboxaldehyde. In 2020.0 ORG BIOMOL CHEM published article about SILYL ENOL ETHERS; CONTIGUOUS QUATERNARY STEREOCENTERS; RADICAL TRIFLUOROMETHYLATION; CATALYZED TRIFLUOROMETHYLATION; AROMATIC-ALDEHYDES; ACYCLIC SYSTEMS; CONSTRUCTION; ACCESS; ALLYLATION; GENERATION in [Terashima, Kyu; Kawasaki-Takasuka, Tomoko; Yamazaki, Takashi] Tokyo Univ Agr & Technol, Inst Engn, Div Appl Chem, 2-24-16 Nakamachi, Koganei, Tokyo 1848588, Japan; [Agou, Tomohiro; Kubota, Toshio] Ibaraki Univ, Dept Biomol Funct Engn, Nakanarusawa 4-12-1, Hitachi, Ibaraki 3168511, Japan in 2020.0, Cited 55.0. The Name is 3-Pyridinecarboxaldehyde. Through research, I have a further understanding and discovery of 500-22-1.
New and successful results for the construction of new and structurally interesting compounds are reportedviaN-heterocyclic carbene (NHC)-catalyzed 1,6-conjugate additions of a variety of aldehydes to delta-CF3-delta-substitutedp-quinone methides generatedin situ, and the products are used for the 1,2-addition reactions of appropriate metal nucleophiles, enabling us to furnish highly diastereoselective products with a unique successive quaternary carbon-tertiary alcohol framework (up to dr = >99 : 1).
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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem