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Efficient Synthesis of Dibenzoxaborininols from Diaryl Ethers and Their Application to Dibenzofuran Synthesis
Author(s) -
Niu Liting,
Yang Haijun,
Jiang Yuyang,
Fu Hua
Publication year - 2013
Publication title -
advanced synthesis and catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.541
H-Index - 155
eISSN - 1615-4169
pISSN - 1615-4150
DOI - 10.1002/adsc.201300567
Subject(s) - dibenzofuran , borylation , chemistry , aryl , palladium , combinatorial chemistry , catalysis , organic chemistry , alkyl
A convenient and efficient method for the borylation of diaryl ethers leading to dibenzoxaborininols and the synthesis of dibenzofuran derivatives has been developed. The borylation involves the sequential three‐step process: lithiation, borylation and hydrolysis. The synthesized dibenzoxaborininols could be readily transformed into dibenzofuran derivatives in good to excellent yields under palladium catalysis in the presence of iodine, and this is the first example for the formation of an aryl CC bond from diarylborinic acids.

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