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

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Metal-Free Synthesis of Indolopyrans and 2,3-Dihydrofurans Based on Tandem Oxidative Cycloaddition

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dc.contributor.author Choi, Subin ko
dc.contributor.author Oh, Hyeonji ko
dc.contributor.author Sim, Jeongwoo ko
dc.contributor.author Yu, Eunsoo ko
dc.contributor.author Shin, Seunghoon ko
dc.contributor.author Park, Cheol-Min ko
dc.date.available 2020-08-21T00:52:58Z -
dc.date.created 2020-08-10 ko
dc.date.issued 2020-07 ko
dc.identifier.citation ORGANIC LETTERS, v.22, no.14, pp.5528 - 5534 ko
dc.identifier.issn 1523-7060 ko
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/47574 -
dc.description.abstract The synthesis of versatile scaffold indolopyrans based on C-C radical-radical cross-coupling under metal-free conditions is described. The reaction involving single electron transfer between coupling partners followed by cage collapse allows highly selective cross-coupling while employing only equimolar amounts of coupling partners. Moreover, the mechanistic manifold was expanded for the functionalization of enamines to give the stereoselective synthesis of 2,3-dihydrofurans. This iodine-mediated oxidative coupling features mild conditions and fast reaction kinetics. ko
dc.language 영어 ko
dc.publisher AMER CHEMICAL SOC ko
dc.title Metal-Free Synthesis of Indolopyrans and 2,3-Dihydrofurans Based on Tandem Oxidative Cycloaddition ko
dc.type ARTICLE ko
dc.identifier.scopusid 2-s2.0-85088097143 ko
dc.identifier.wosid 000551552600048 ko
dc.type.rims ART ko
dc.identifier.doi 10.1021/acs.orglett.0c01896 ko
dc.identifier.url https://pubs.acs.org/doi/10.1021/acs.orglett.0c01896 ko
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