One-step synthesis of tetrahydroindoles by ceric(IV) ammonium nitrate-promoted oxidative cycloaddition of enaminones and vinyl ethers

Title
One-step synthesis of tetrahydroindoles by ceric(IV) ammonium nitrate-promoted oxidative cycloaddition of enaminones and vinyl ethers
Author(s)
이용록타이벳흥김성홍[김성홍]
Keywords
FURONAPHTHOQUINONE NATURAL-PRODUCTS; EFFICIENT SYNTHESIS; 1,3-DICARBONYL COMPOUNDS; GENERAL-SYNTHESIS; INDOLES; 4-OXO-4,5,6,7-TETRAHYDROINDOLES; DIHYDROFURANS; HETEROCYCLES; ROUTE; 4,5,6,7-TETRAHYDROINDOLES
Issue Date
201410
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
TETRAHEDRON, v.70, no.43, pp.8108 - 8113
Abstract
A new and general one-step procedure to synthesize a variety of biologically interesting tetrahydroindole derivatives was successfully devised by reacting various beta-enaminones with vinyl ethers in the presence of ceric(IV) ammonium nitrate as promoter. This novel synthetic method provides a facile and promising strategy to various tetrahydroindole derivatives in moderate to good yields. (C) 2014 Elsevier Ltd. All rights reserved.
URI
http://hdl.handle.net/YU.REPOSITORY/30644http://dx.doi.org/10.1016/j.tet.2014.08.011
ISSN
0040-4020
Appears in Collections:
공과대학 > 화학공학부 > Articles
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