A Journey through Hemetsberger–Knittel , Leimgruber–Batcho and Bartoli Reactions: Access to Several Hydroxy 5‐ and 6‐Azaindoles-Reference-Cited by-同舟云学术

A Journey through Hemetsberger–Knittel , Leimgruber–Batcho and Bartoli Reactions: Access to Several Hydroxy 5‐ and 6‐Azaindoles

Published:2022-02-04 Issue: Volume: Page:
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:en
Short-container-title:Helvetica Chimica Acta

Author:

Radix Sylvie¹²^ORCID,Hallé François²^ORCID,Mahiout Zahia¹,Teissonnière Amélie¹,Bouchez Grégoire¹,Auberger Ludovic¹,Barret Roland¹,Lomberget Thierry¹²^ORCID

Affiliation:

1. Université de Lyon Université Lyon 1 Faculté de Pharmacie, ISPB, EA 4446 Bioactive Molecules and Medicinal Chemistry FR-69373 Lyon Cedex 08 France

2. Université de Lyon Université Lyon 1 CNRS UMR 5246 Institut de Chimie et Biochimie Moléculaires et Supramoléculaires (ICBMS) Faculté de Pharmacie-ISPB, 8 Avenue Rockefeller FR-69373 Lyon Cedex 08 France

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/hlca.202100211

Reference62 articles.

1. ‘Azaindoles therapeutic agents’;Motati D. R.;Bioorg. Med. Chem.,2020

2. The Azaindole Framework in the Design of Kinase Inhibitors

3. Synthesis and reactivity of 4-, 5- and 6-azaindoles

4. Synthesis and reactivity of 7-azaindole (1H-pyrrolo[2,3-b]pyridine)

5. Organometallic methods for the synthesis and functionalization of azaindoles

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