BROWSE

Related Researcher

Author's Photo

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

ITEM VIEW & DOWNLOAD

Electrosynthesis of Dihydropyrano[4,3‐b ]indoles Based on a Double Oxidative [3+3] Cycloaddition

DC Field Value Language
dc.contributor.author Choi, Subin ko
dc.contributor.author Park, Jinhwi ko
dc.contributor.author Yu, Eunsoo ko
dc.contributor.author Sim, Jeongwoo ko
dc.contributor.author Park, Cheol-Min ko
dc.date.available 2020-06-08T01:37:46Z -
dc.date.created 2020-06-01 ko
dc.date.issued 2020-05 ko
dc.identifier.citation ANGEWANDTE CHEMIE-INTERNATIONAL EDITION ko
dc.identifier.issn 1433-7851 ko
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/32301 -
dc.description.abstract Oxidative [3+3] cycloadditions offer an efficient route for six-membered-ring formation. This approach has been realized based on an electrochemical oxidative coupling of indoles/enamines with active methylene compounds followed by tandem 6 pi-electrocyclization leading to the synthesis of dihydropyrano[4,3-b]indoles and 2,3-dihydrofurans. The radical-radical cross-coupling of the radical species generated by anodic oxidation combined with the cathodic generation of the base from O-2 allows for mild reaction conditions for the synthesis of structurally complex heterocycles. ko
dc.language 영어 ko
dc.publisher WILEY-V C H VERLAG GMBH ko
dc.title Electrosynthesis of Dihydropyrano[4,3‐b ]indoles Based on a Double Oxidative [3+3] Cycloaddition ko
dc.type ARTICLE ko
dc.identifier.scopusid 2-s2.0-85084800306 ko
dc.identifier.wosid 000533313000001 ko
dc.type.rims ART ko
dc.identifier.doi 10.1002/ange.202003364 ko
dc.identifier.url https://onlinelibrary.wiley.com/doi/full/10.1002/ange.202003364 ko
Appears in Collections:
PHY_Journal Papers

find_unist can give you direct access to the published full text of this article. (UNISTARs only)

Show simple item record

qrcode

  • mendeley

    citeulike

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

MENU