Regioselective Synthesis of Highly Functionalized Furans Through the Ru-II-Catalyzed [3+2] Cycloaddition of Diazodicarbonyl Compounds

Title
Regioselective Synthesis of Highly Functionalized Furans Through the Ru-II-Catalyzed [3+2] Cycloaddition of Diazodicarbonyl Compounds
Author(s)
이용록하립개
Keywords
ONE-POT SYNTHESIS; H INSERTION REACTION; ELECTRON-DEFICIENT ALKYNES; DIAZO-TRANSFER REACTIONS; FREE-RADICAL REACTIONS; ONE-STEP SYNTHESIS; EFFICIENT SYNTHESIS; 1,3-DICARBONYL COMPOUNDS; POLYSUBSTITUTED FURANS; SUBSTITUTED FURANS
Issue Date
201406
Publisher
WILEY-V C H VERLAG GMBH
Citation
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, v.2014, no.16, pp.3430 - 3442
Abstract
A novel method for the Ru-II-catalyzed regioselective synthesis of highly functionalized furans from readily available cyclic and acyclic diazodicarbonyl compounds and terminal alkynes is described. The devised protocol offers a straight-forward means to the construction of a variety of diverse furan derivatives through powerful cascade processes, including the formation of ruthenium carbenoid, cyclopropenation, ring-opening metathesis, and cyclization.
URI
http://hdl.handle.net/YU.REPOSITORY/32024http://dx.doi.org/10.1002/ejoc.201402067
ISSN
1434-193X
Appears in Collections:
공과대학 > 화학공학부 > Articles
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML


qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE