Indole-ynones as Privileged Substrates for Radical Dearomatizing Spirocyclization Cascades-Reference-Cited by-同舟云学术

Indole-ynones as Privileged Substrates for Radical Dearomatizing Spirocyclization Cascades

Published:2022-01-05 Issue:2 Volume:24 Page:668-674
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Inprung Nantachai¹,Ho Hon Eong¹^ORCID,Rossi-Ashton James A.¹^ORCID,Epton Ryan G.¹^ORCID,Whitwood Adrian C.¹^ORCID,Lynam Jason M.¹^ORCID,Taylor Richard J. K.¹,James Michael J.¹^ORCID,Unsworth William P.¹^ORCID

Affiliation:

1. Department of Chemistry, University of York, Heslington, York, YO10 5DD, U.K.

Funder

Leverhulme Trust

University of York

Royal Thai Government

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c04098

Reference63 articles.

1. Synthesis of Natural-Product-Like Molecules with Over Eighty Distinct Scaffolds

2. Natural product derived privileged scaffolds in drug discovery

3. Spiroindolones, a Potent Compound Class for the Treatment of Malaria

4. Transition‐Metal‐Mediated Routes to 3,3‐Disubstituted Oxindoles through Anilide Cyclisation

5. Metal-Catalyzed Approaches toward the Oxindole Core

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