Efficient one-pot synthesis of biologically interesting diverse furo [2,3-b]pyran-6-ones by rhodium(II)-catalyzed cascade reactions of diazo compound with ethynyl compounds

Title
Efficient one-pot synthesis of biologically interesting diverse furo [2,3-b]pyran-6-ones by rhodium(II)-catalyzed cascade reactions of diazo compound with ethynyl compounds
Author(s)
이용록소마이마가크리쉬나김성홍[김성홍]
Keywords
PENICILLIUM-BREVICOMPACTUM DIERCKX; CYCLIC DIAZODICARBONYL COMPOUNDS; SUBSTITUTED ALPHA-HALOENONES; WOLFF REARRANGEMENT; CONJUGATED POLYMERS; ALKYLATION REACTION; MELDRUMS ACID; RING-SYSTEM; WAOL-B; DERIVATIVES
Issue Date
201311
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
TETRAHEDRON, v.69, no.44, pp.9294 - 9302
Abstract
Rhodium(II)-catalyzed reactions of diazo out. These reactions provide a rapid route one-pot via cascade reactions of metal expansion. compound and a variety of ethynyl compounds were carried for preparing a variety of furo[2,3-b]pyran-6-one derivatives in carbenoid reaction/ketene formation/[2+2]cycloaddition/ring (C) 2013 Elsevier Ltd. All rights reserved.
URI
http://hdl.handle.net/YU.REPOSITORY/28630http://dx.doi.org/10.1016/j.tet.2013.08.054
ISSN
0040-4020
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