Copper‐Promoted N‐Arylation of the Imidazole Side Chain of Protected Histidine by Using Triarylbismuth Reagents-Reference-Cited by-同舟云学术

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Copper‐Promoted N‐Arylation of the Imidazole Side Chain of Protected Histidine by Using Triarylbismuth Reagents

Published:2021-08-06 Issue:53 Volume:27 Page:13330-13336
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Chan Hwai‐Chien¹,Bueno Bianca¹,Le Roch Adrien¹,Gagnon Alexandre¹^ORCID

Affiliation:

1. Université du Québec à Montréal Département de chimie C.P. 8888, Succursale Centre-Ville Montréal Québec H3C 3P8 Canada

Funder

Natural Sciences and Engineering Research Council of Canada

Boehringer Ingelheim

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202102186

Reference56 articles.

1. Green bismuth

2.

3. Recent Research Trends on Bismuth Compounds in Cancer Chemoand Radiotherapy

4. Review: Bismuth complexes: synthesis and applications in biomedicine

5. Current and Potential Applications of Bismuth-Based Drugs

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3. High efficient copper-promoted N-arylation of secondary and primary amines with triarylbismuth reagents under mild conditions;Journal of Molecular Structure;2023-12

4. On the Barton Copper‐Catalyzed C3‐Arylation of Indoles using Triarylbismuth bis(trifluoroacetate) Reagents;ChemPlusChem;2023-03-15

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