상세 보기
초록
An efficient synthetic method to access ethyl arylpropiolates has been developed; it involves a palladium-catalyzed cross-coupling reaction between a wide range of aryl iodides and lithium tetrakis(ethoxycarbonylethynyl)indates (0.35 equiv) generated in situ from indium trichloride and alkynides obtained from ethyl propiolate and n-butyllithium.
키워드
cross-coupling; palladium; indium; lithium tetrakis(ethoxycarbonylethynyl)indate; propiolates; catalysis; ONE-POT; ARYLBORONIC ACIDS; TRIORGANOINDIUM REAGENTS; 2-ARYL 2,3-ALKADIENOATES; INDIUM ORGANOMETALLICS; TERMINAL ALKYNES; ALLYL ACETATES; VINYL HALIDES; LIGAND-FREE; DERIVATIVES
- 제목
- Synthesis of Ethyl Arylpropiolates through Palladium-Catalyzed Cross-Coupling Reactions of Aryl Iodides with In Situ Generated Lithium Tetrakis(ethoxycarbonylethynyl)indates
- 저자
- Park, Youngchul; Kang, Dongjin; Jeon, Woo Hyung; Ryu, Taekyu; Lee, Phil Ho
- 발행일
- 2014-09
- 유형
- Article
- 저널명
- Synthesis
- 권
- 46
- 호
- 17
- 페이지
- 2305 ~ 2311