AgOTf and TfOH co-catalyzed isoquinoline synthesis via redox reactions of O-alkyl oximes

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WEB OF SCIENCE

48
Citations

SCOPUS

50

초록

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.

키워드

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
DOI
10.1016/j.tetlet.2009.02.144
발행일
2009-05
유형
Article
저널명
Tetrahedron Letters
권
50
호
20
페이지
2305 ~ 2308