Synthesis of the First Expanded Carbaporphyrinoid by the “4 + 1” Approach-Reference-Cited by-同舟云学术

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Synthesis of the First Expanded Carbaporphyrinoid by the “4 + 1” Approach

Published:1998-09-01 Issue:38 Volume:120 Page:9965-9966
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Lash Timothy D.¹,Richter Daniel T.¹

Affiliation:

1. Department of Chemistry Illinois State University Normal, Illinois 61790-4160

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja981887q

Reference21 articles.

1. Sapphyrins: novel aromatic pentapyrrolic macrocycles

2. Sulphur extrusion reactions applied to the synthesis of corroles and related systems

3. Sessler, J. L.; Cyr, M. J.; Burrel, A. K.Tetrahedron1992,48, 9661.

4. Protonation of 5,10,15,20-tetraphenylsapphyrin—identification of inverted and planar dicationic forms

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1. Organometallic Chemistry within the Structured Environment Provided by the Macrocyclic Cores of Carbaporphyrins and Related Systems;Molecules;2023-02-03

2. Synthesis of Doubly Fused Phenothiazine-Embedded Dithiasapphyrins;The Journal of Organic Chemistry;2022-11-10

3. Theoretical analysis of expanded porphyrins: Aromaticity, stability, and optoelectronic properties;Frontiers in Chemistry;2022-09-01

4. Tailor-made aromatic porphyrinoids with NIR absorption;Chemical Communications;2022

5. Extended porphyrinoid chromophores: heteroporphyrins fused to phenanthrene and acenaphthylene;Tetrahedron;2021-11

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