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AgOTf and TfOH co-catalyzed isoquinoline synthesis via redox reactions of O-alkyl oximes
- Hwang, Soojin;
- Lee, Youngun;
- Lee, Phil Ho;
- Shin, Seunghoon
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Under AgOTf and Bronsted acid co-catalysis, O-alkyl o-alkynylbenzaldoxime derivatives undergo a cyclization-induced N-O cleavage to produce isoquinolines with the simultaneous oxidation of O-alkyl group. This redox-based method provides a general access to diverse isoquinoline-derived heterocycles that are simple, efficient, and tolerant of various functional groups from readily available and hydrolytically stable oxime precursors.
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HIGHLY EFFICIENT; CYCLIZATION; ALDOXIMES; PYRIDINES; CYCLOISOMERIZATION; GENERATION; IMINES; ETHERS; ROUTE; WATER
- 제목
- AgOTf and TfOH co-catalyzed isoquinoline synthesis via redox reactions of O-alkyl oximes
- 저자
- Hwang, Soojin; Lee, Youngun; Lee, Phil Ho; Shin, Seunghoon
- 발행일
- 2009-05
- 유형
- Article
- 권
- 50
- 호
- 20
- 페이지
- 2305 ~ 2308