13391-27-0Relevant articles and documents
Synthesis of benzofurans via Pd2+-catalyzed oxidative cyclization of 2-allylphenols
Roshchin, Alexander I.,Kel'chevski, Sergey M.,Bumagin, Nikolai A.
, p. 163 - 167 (1998)
Substituted 2-methylbenzofurans were obtained from 2-allylphenols via Pd2+-catalyzed oxidative cyclization using Cu(OAc)2-LiCl as a reoxidant and wet DMF as a solvent.
Preparation of substituted hydroquinones and benzofurans from 1,4-quinone monoketals
Salom-Roig, Xavier J.,Renaud, Philippe
, p. 3419 - 3424 (2006)
An easy procedure for the preparation of 2-substituted hydroquinones, by addition of organolithium or organomagnesium compounds to 1,4-quinone monoketals followed by acid-catalyzed dienone-phenol type rearrangement, is described. Transformation of the pro
TRICYCLIC SUBSTITUTED PIPERIDINE DIONE COMPOUND
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Paragraph 0107; 0110, (2021/07/17)
Disclosed is a series of tricyclic substituted piperidine dione compounds, and applications thereof in the preparation of medicines for treating diseases related to CRBN protein; specifically disclosed are the derivative compound represented by formula (I) or a pharmaceutically acceptable salt thereof.
Synthesis of Benzo[ b]furans by Intramolecular C-O Bond Formation Using Iron and Copper Catalysis
Henry, Martyn C.,Sutherland, Andrew
, p. 2766 - 2770 (2020/03/30)
One-pot processes for the synthesis of benzo[b]furans from 1-aryl- or 1-alkylketones using nonprecious transition metal catalysts have been developed. Regioselective iron(III)-catalyzed halogenation of the aryl ring, followed by iron- or copper-catalyzed O-arylation allowed the synthesis of various structural analogues, including the benzo[b]furan-derived natural products corsifuran C, moracin F, and caleprunin B.
