Indole Editing Enabled by HFIP‐Mediated Ring‐Switch Reactions of 3‐Amino‐2‐Hydroxyindolines-Reference-Cited by-同舟云学术

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Indole Editing Enabled by HFIP‐Mediated Ring‐Switch Reactions of 3‐Amino‐2‐Hydroxyindolines

Published:2022-05-19 Issue:37 Volume:28 Page:
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chemistry A European J

Author:

Abe Takumi¹^ORCID,Yamashiro Toshiki¹^ORCID,Shimizu Kaho¹,Sawada Daisuke¹^ORCID

Affiliation:

1. Graduate School of Medicine Dentistry and Pharmaceutical Sciences Okayama University 1-1-1 Tsushima-naka, Kita-ku Okayama 7008530 Japan

Funder

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202201113

Reference78 articles.

1.

2. Indoles — A promising scaffold for drug development

3. Marine Indole Alkaloids: Potential New Drug Leads for the Control of Depression and Anxiety

4.

5. Catalytic Functionalization of Indoles in a New Dimension

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1. Formal One Carbon Deletion of Indoline Hemiaminals under Tautomeric Control to Access 2-Aminobenzyl Compounds;The Journal of Organic Chemistry;2024-07-01

2. On Demand Synthesis of C3−N1’ Bisindoles by a Formal Umpolung Strategy: First Total Synthesis of (±)‐Rivularin A;Chemistry – A European Journal;2024-01-08

3. Switchable synthesis of 3-aminoindolines and 2′-aminoarylacetic acids using Grignard reagents and 3-azido-2-hydroxyindolines;Chemical Communications;2024

4. Synthetic strategies for the construction of C3–N1′ bisindoles;Organic & Biomolecular Chemistry;2024

5. Indoline hemiaminals: a platform for accessing anthranilic acid derivatives through oxidative deformylation;Organic & Biomolecular Chemistry;2024

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