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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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. (C) 2009 Elsevier Ltd. All rights reserved.

키워드

HIGHLY EFFICIENTCYCLIZATIONALDOXIMESPYRIDINESCYCLOISOMERIZATIONGENERATIONIMINESETHERSROUTEWATER
제목
AgOTf and TfOH co-catalyzed isoquinoline synthesis via redox reactions of O-alkyl oximes
저자
Hwang, SoojinLee, YoungunLee, Phil HoShin, Seunghoon
DOI
10.1016/j.tetlet.2009.02.144
발행일
2009-05-20
유형
Article
저널명
Tetrahedron Letters
50
20
페이지
2305 ~ 2308