Nickel-catalyzed cross-coupling of bromophenols with Grignard reagents in the solid phase synthesis

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초록

Polymer-bound substituted bromophenols were found to readily undergo a Ni(0)-catalyzed cross-coupling reaction with Grignard reagents to give a variety of substituted phenols and hydroquinones, after cleavage from the support, in moderate to high yields. The requisite bromophenol derivatives, which were prepared from the corrresponding phenols and hydroquinone using BTMA Br-3 or TBA Br-3, were attached to the solid support by the Mitsunobu reaction.

키워드

bromophenols; carbon-carbon cross-coupling; Grignard reagents; nickel catalyst; solid phase organic synthesis; substituted hydroquinones; substituted phenols; DIRECTED ORTHO-METALATION; C-C BOND; HECK REACTION; MITSUNOBU REACTION; PEPTIDE-SYNTHESIS; LINKER APPROACH; STILLE REACTION; SUZUKI; SUPPORT; BIARYL
제목
Nickel-catalyzed cross-coupling of bromophenols with Grignard reagents in the solid phase synthesis
저자
Park, Heon; Yoon, Sang-Il; Park, Kwangyong; Lee, Yoon-Sik
DOI
10.1023/A:1013853421101
발행일
2000-06
유형
Article
저널명
Molecular Diversity
권
5
호
2
페이지
57 ~ 60