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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 Pyridines by Carbenoid-Mediated Ring Opening of 2H-Azirines

DC Field Value Language
dc.contributor.author Loy, Nicole S. Y. ko
dc.contributor.author Singh, Alok ko
dc.contributor.author Xu, Xianxiu ko
dc.contributor.author Park, Cheol-Min ko
dc.date.available 2014-11-11T00:15:50Z -
dc.date.created 2014-11-10 ko
dc.date.issued 2013-02 -
dc.identifier.citation ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.52, no.8, pp.2212 - 2216 ko
dc.identifier.issn 1433-7851 ko
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/8536 -
dc.identifier.uri http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84873909860 ko
dc.description.abstract Roaming the range: The title reaction tolerates a wide range of substituents on the resulting pyridine ring using mild reaction conditions (see scheme; esp=α,α,α′,α′-tetramethyl-1,3- benzenedipropionic acid). The formation of the key intermediate is catalyst-controlled, and subsequent cyclization and oxidation affords pyridines in excellent yields. The method has been used for the efficient synthesis of polyarylpyridines. ko
dc.description.statementofresponsibility close -
dc.language ENG ko
dc.publisher WILEY-V C H VERLAG GMBH ko
dc.subject carbenoids ko
dc.subject electrocyclic reactions ko
dc.subject heterocycle ko
dc.subject ring expansion ko
dc.subject synthetic methods ko
dc.title Synthesis of Pyridines by Carbenoid-Mediated Ring Opening of 2H-Azirines ko
dc.type ARTICLE ko
dc.identifier.scopusid 2-s2.0-84873909860 ko
dc.identifier.wosid 000314998500013 ko
dc.type.rims ART ko
dc.description.wostc 26 *
dc.description.scopustc 16 *
dc.date.tcdate 2015-05-06 *
dc.date.scptcdate 2014-11-10 *
dc.identifier.doi 10.1002/anie.201209301 ko
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