Aromaticity of topological isomers of cyclazines and their [14] to [18] annulenes-Reference-Cited by-同舟云学术

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Aromaticity of topological isomers of cyclazines and their [14] to [18] annulenes

Published:2011-02 Issue:2-3 Volume:963 Page:525-532
ISSN:2210-271X
Container-title:Computational and Theoretical Chemistry
language:en
Short-container-title:Computational and Theoretical Chemistry

Author:

Fallah-Bagher-Shaidaei Hossein,Farkhonde Reza,Navideh Leila Ghalandari

Publisher

Elsevier BV

Subject

Physical and Theoretical Chemistry,Condensed Matter Physics,Biochemistry

Reference89 articles.

1. Cyclazines. A New Class of Aromatic Heterocycles1

2. BN-Doped Fullerenes: An NICS Characterization

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1. Theoretical study on the conformation and aromaticity of [13] to [33] double-stranded cyclophanes encompassing three benzene subunits;Structural Chemistry;2024-05-30

2. Oxidative Cyclodehydrogenation of Trinaphthylamine: Selective Formation of a Nitrogen‐Centered Polycyclic π‐System Comprising 5‐ and 7‐Membered Rings;Angewandte Chemie International Edition;2022-08-24

3. Oxidative Cyclodehydrogenation of Trinaphthylamine: Selective Formation of a Nitrogen‐Centered Polycyclic π‐System Comprising 5‐ and 7‐Membered Rings;Angewandte Chemie;2022-08-24

4. Cyclazines‐Structure and Aromaticity or Antiaromaticity on the Magnetic Criterion;European Journal of Organic Chemistry;2022-02-22

5. Three Heterocyclic Rings Fused (5-5-5);Comprehensive Heterocyclic Chemistry IV;2022

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