Synthesis of Unsymmetrical o-Biphenols and o-Binaphthols via Silicon-Tethered Pd-Catalyzed C-H Arylation

被引:35
|
作者
Huang, Chunhui [1 ]
Gevorgyan, Vladimir [1 ]
机构
[1] Univ Illinois, Dept Chem, Chicago, IL 60607 USA
基金
美国国家卫生研究院;
关键词
PROTON-ABSTRACTION MECHANISM; INTRAMOLECULAR ARYLATION; PHOSPHORAMIDITE LIGANDS; CONJUGATE ADDITION; COUPLING REACTION; NATURAL-PRODUCTS; PHENOLS; 2-NAPHTHOLS; COMPLEXES; 2,2'-BIPHENOL;
D O I
10.1021/ol100924n
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A mild, practical, and efficient method for the synthesis of unsymmetrical o-biphenols (including o-phenol-naphthols and o-binaphthols) has been developed. Unsymmetrical bis-aryloxy silanes, which were readily prepared in a semi-one-pot fashion, underwent the Pd-catalyzed intramolecular arylation followed by a routine TBAF desilylation step to furnish valuable unsymmetrical biphenols without necessity of isolation of seven-membered intermediates. The excellent functional group tolerance allows for synthesis of a variety of functionalized o-biphenols and o-binaphthols from easily available staring materials.
引用
收藏
页码:2442 / 2445
页数:4
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