Formula: C8H8O2. In 2019 J AM CHEM SOC published article about REGIOSELECTIVE ADDITION; NUCLEOPHILIC-ADDITION; BOND ACTIVATION; COMPLEXES; ALLENYL; ETHERS; ARYL; CYCLOADDITION; CYCLIZATION; REACTIVITY in [Ishida, Naoki; Hori, Yusaku; Okumura, Shintaro; Murakami, Masahiro] Kyoto Univ, Dept Synthet Chem & Biol Chem, Kyoto 6158510, Japan in 2019, Cited 45. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4.
A convenient method for the synthesis of 1,3-dienes from readily available compounds is reported. 2-Aryoxy-1,3-dienes are produced stereoselectively by a nickel-catalyzed reaction of propargyl carbonates with phenols. Functional group tolerance is broad to allow iodo, formyl, and boryl groups. The resulting 1,3-dienes are of much synthetic value because they can participate in a wide variety of reactions, including the Diels Alder reaction.
Formula: C8H8O2. About 4′-Hydroxyacetophenone, If you have any questions, you can contact Ishida, N; Hori, Y; Okumura, S; Murakami, M or concate me.
Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles