Synthesis of 2-aminofurans and 2-unsubstituted furans via carbenoid-mediated [3 + 2] cycloaddition

An efficient dual synthetic manifold for 2-aminofurans and 2-unsubstituted furans has been developed. The carbenoid-mediated [3 + 2] cycloaddition of copper carbenoids with enamines provides 2-amino-2,3-dihydrofurans which serve as common intermediates for both 2-aminofurans and 2-unsubstituted fura...

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Main Authors:	Jiang, Yaojia, Khong, Vanessa Zhong Yue, Lourdusamy, Emmanuvel, Park, Cheol-Min
Other Authors:	School of Physical and Mathematical Sciences
Format:	Article
Language:	English
Published:	2013
Online Access:	https://hdl.handle.net/10356/101492 http://hdl.handle.net/10220/11103
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Institution:	Nanyang Technological University
Language:	English

id	sg-ntu-dr.10356-101492
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spelling	sg-ntu-dr.10356-1014922020-03-07T12:34:50Z Synthesis of 2-aminofurans and 2-unsubstituted furans via carbenoid-mediated [3 + 2] cycloaddition Jiang, Yaojia Khong, Vanessa Zhong Yue Lourdusamy, Emmanuvel Park, Cheol-Min School of Physical and Mathematical Sciences An efficient dual synthetic manifold for 2-aminofurans and 2-unsubstituted furans has been developed. The carbenoid-mediated [3 + 2] cycloaddition of copper carbenoids with enamines provides 2-amino-2,3-dihydrofurans which serve as common intermediates for both 2-aminofurans and 2-unsubstituted furans. 2013-07-10T06:02:02Z 2019-12-06T20:39:14Z 2013-07-10T06:02:02Z 2019-12-06T20:39:14Z 2012 2012 Journal Article Jiang, Y., Khong, V. Z. Y., Lourdusamy, E., Park, C.-M. (2012). Synthesis of 2-aminofurans and 2-unsubstituted furans via carbenoid-mediated [3 + 2] cycloaddition. Chemical Communications, 48(25), 3133-3135. https://hdl.handle.net/10356/101492 http://hdl.handle.net/10220/11103 10.1039/c2cc18139h en Chemical communications © 2012 The Royal Society of Chemistry.
institution	Nanyang Technological University
building	NTU Library
country	Singapore
collection	DR-NTU
language	English
description	An efficient dual synthetic manifold for 2-aminofurans and 2-unsubstituted furans has been developed. The carbenoid-mediated [3 + 2] cycloaddition of copper carbenoids with enamines provides 2-amino-2,3-dihydrofurans which serve as common intermediates for both 2-aminofurans and 2-unsubstituted furans.
author2	School of Physical and Mathematical Sciences
author_facet	School of Physical and Mathematical Sciences Jiang, Yaojia Khong, Vanessa Zhong Yue Lourdusamy, Emmanuvel Park, Cheol-Min
format	Article
author	Jiang, Yaojia Khong, Vanessa Zhong Yue Lourdusamy, Emmanuvel Park, Cheol-Min
spellingShingle	Jiang, Yaojia Khong, Vanessa Zhong Yue Lourdusamy, Emmanuvel Park, Cheol-Min Synthesis of 2-aminofurans and 2-unsubstituted furans via carbenoid-mediated [3 + 2] cycloaddition
author_sort	Jiang, Yaojia
title	Synthesis of 2-aminofurans and 2-unsubstituted furans via carbenoid-mediated [3 + 2] cycloaddition
title_short	Synthesis of 2-aminofurans and 2-unsubstituted furans via carbenoid-mediated [3 + 2] cycloaddition
title_full	Synthesis of 2-aminofurans and 2-unsubstituted furans via carbenoid-mediated [3 + 2] cycloaddition
title_fullStr	Synthesis of 2-aminofurans and 2-unsubstituted furans via carbenoid-mediated [3 + 2] cycloaddition
title_full_unstemmed	Synthesis of 2-aminofurans and 2-unsubstituted furans via carbenoid-mediated [3 + 2] cycloaddition
title_sort	synthesis of 2-aminofurans and 2-unsubstituted furans via carbenoid-mediated [3 + 2] cycloaddition
publishDate	2013
url	https://hdl.handle.net/10356/101492 http://hdl.handle.net/10220/11103
_version_	1681048220472442880

Synthesis of 2-aminofurans and 2-unsubstituted furans via carbenoid-mediated [3 + 2] cycloaddition

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