Rh(II)-Catalyzed Synthetic Strategy for Diverse and Functionalized Halonaphthalenyl Ethers and Esters from Diazo Compounds and Its Application to Polyaromatic Compounds

被引:13
作者
Baral, Ek Raj [1 ]
Lee, Yong Rok [1 ]
Kim, Sung Hong [2 ]
Wee, Young-Jung [3 ]
机构
[1] Yeungnam Univ, Sch Chem Engn, Kyongsan 712749, South Korea
[2] Korea Basic Sci Inst, Anal Res Div, Daegu Ctr, Taegu 702701, South Korea
[3] Yeungnam Univ, Dept Food Sci & Technol, Kyongsan 712749, South Korea
来源
SYNTHESIS-STUTTGART | 2016年 / 48卷 / 04期
关键词
diazo compounds; rhodium(II) catalyst; halonaphthalenyl ethers; halonaphthalenyl esters; polyaromatic compounds; ONE-POT SYNTHESIS; SUBSTITUTED ALPHA-HALOENONES; THERMAL CASCADE REACTIONS; DIAZODICARBONYL COMPOUNDS; REGIOSELECTIVE HALOGENATION; EFFICIENT SYNTHESIS; AROMATIC-COMPOUNDS; COUPLING REACTIONS; 3+2 CYCLOADDITION; BROMINATION;
D O I
10.1055/s-0035-1561295
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An efficient and simple synthesis of various functionalized halonaphthalenyl ethers and esters in moderate to good yield was achieved via rhodium(II)-catalyzed reaction of readily available diazo compounds with benzyl halides or acid halides. This methodology has several advantages, such as ease of handling, mild reaction conditions, bromine- or chlorine-free route, and the use of an effective catalyst. The synthesized compounds were further converted into valuable polyaromatic compounds using the Suzuki reaction.
引用
收藏
页码:579 / 587
页数:9
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