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Park, Cheol-Min
Synthetic & Medicinal Chemistry Lab
Research Interests
  • Organic synthesis, medicinal chemistry, chemical biology

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

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dc.contributor.author Jiang, Yaojia ko
dc.contributor.author Khong, Vanessa Zhong Yue ko
dc.contributor.author Lourdusamy, Emmanuvel ko
dc.contributor.author Park, Cheol-Min ko
dc.date.available 2014-11-11T00:12:18Z -
dc.date.created 2014-11-10 ko
dc.date.issued 2012-03 -
dc.identifier.citation CHEMICAL COMMUNICATIONS, v.48, no.25, pp.3133 - 3135 ko
dc.identifier.issn 1359-7345 ko
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/8488 -
dc.identifier.uri http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84863264743 ko
dc.description.abstract 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. ko
dc.description.statementofresponsibility close -
dc.language ENG ko
dc.publisher ROYAL SOC CHEMISTRY ko
dc.subject POLYSUBSTITUTED FURANS ko
dc.subject EFFICIENT SYNTHESIS ko
dc.subject HETEROCYCLES ko
dc.subject DERIVATIVES ko
dc.subject PYRROLES ko
dc.subject KETONES ko
dc.subject ETHERS ko
dc.title Synthesis of 2-aminofurans and 2-unsubstituted furans via carbenoid-mediated [3+2] cycloaddition ko
dc.type ARTICLE ko
dc.identifier.scopusid 2-s2.0-84863264743 ko
dc.identifier.wosid 000300782600029 ko
dc.type.rims ART ko
dc.description.wostc 14 *
dc.description.scopustc 13 *
dc.date.tcdate 2015-05-06 *
dc.date.scptcdate 2014-11-10 *
dc.identifier.doi 10.1039/c2cc18139h ko
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