Synthesis of neopentyl biphenyisulfonates using the Suzuki-Miyaura reaction

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6

초록

Palladium-catalyzed cross-coupling reactions of neopentyloxysulfonylphenyl bromides with arylboronic acids provided a variety of neopentyl biphenylsulfonates in good yields. 2-Bromo- and 4-bromobenzenesulfonates underwent the coupling reaction more rapidly than 3-bromobenzenesulfonate, while chlorobenzenesulfonate did not produce the coupling product under the standard reaction conditions.

키워드

cross-coupling; bromobenzenesulfonates; biphenylsulfonates; arylboronic acid; Suzuki-Miyaura reaction; CROSS-COUPLING REACTIONS; DIRECTED ORTHO-METALATION; ARYL GRIGNARD-REAGENTS; C BOND FORMATION; ARYLBORONIC ACIDS; SOLID SUPPORT; ORGANIC ELECTROPHILES; BIARYL SYNTHESIS; NICKEL; DERIVATIVES
제목
Synthesis of neopentyl biphenyisulfonates using the Suzuki-Miyaura reaction
저자
Cho, Chul-Hee; Kim, Chul-Bae; Sun, Myungchul; Park, Kwangyong
DOI
10.5012/bkcs.2003.24.11.1632
발행일
2003-11
유형
Article
저널명
Bulletin of the Korean Chemical Society
권
24
호
11
페이지
1632 ~ 1636