Synthesis and Relative Diatropicity of a Remarkably Aromatic Thia[13]annulene-Reference-Cited by-同舟云学术

Synthesis and Relative Diatropicity of a Remarkably Aromatic Thia[13]annulene

Published:1996-01-01 Issue:4 Volume:118 Page:722-726
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Mitchell Reginald H.¹,Iyer Vivekanantan S.¹

Affiliation:

1. Contribution from the Department of Chemistry, University of Victoria, PO Box 3055, Victoria, British Columbia, Canada V8W 3P6

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja953025k

Reference26 articles.

1. For a recent review see: Minkin, V. J.; Glukhovtsev, M. N.; Simkin, B. Y.Aromaticityand Antiaromaticity: Electronic and Structural Aspects.Wiley. New York; 1994.

2. Aromaticity and Antiaromaticity in Five-Membered C4H4X Ring Systems:“Classical” and“Magnetic” Concepts May Not Be“Orthogonal”

3. The Synthesis of Tetradehydrocyclotetradeca[c]furans(?Didehydro[14]annuleno[c]furans?), 18 ?-Electron Analogs of Isobenzofuran

4. Aza[17]annulenes

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