A New Synthetic Approach to N-Arylquinolino[2,3,4-at]porphyrins from β-Arylaminoporphyrins-Reference-Cited by-同舟云学术

A New Synthetic Approach to N-Arylquinolino[2,3,4-at]porphyrins from β-Arylaminoporphyrins

Published:2008-08-22 Issue:18 Volume:73 Page:7353-7356
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Pereira Ana M. V. M.¹,Alonso Cristina M. A.¹,Neves Maria G. P. M. S.¹,Tomé Augusto C.¹,Silva Artur M. S.¹,Paz Filipe A. A.¹,Cavaleiro José A. S.¹

Affiliation:

1. Department of Chemistry, University of Aveiro, 3810-193 Aveiro, Portugal, and Department of Chemistry, CICECO, University of Aveiro, 3810-193 Aveiro, Portugal

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo800975c

Reference30 articles.

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2. Substituent effects in the electroreduction of porphyrins and metalloporphyrins

3. Efficient peripheral functionalization of porphyrins

4. Reaction of metallo-2-nitro-5,10,15,20-tetraphenylporphyrins with oxyanions. Temperature-dependent competition between nucleophilic addition and single-electron transfer processes

5. Solvent-dependent ambident nucleophilicity of phenoxide ion towards nitroporphyrins: synthesis of 2-hydroxyaryl- and 2-aryloxy-5,10,15,20-tetraphenylporphyrins by displacement of a nitro group

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