The imbalanced kekule structure contributions in the ring in 1,3,5-trisubstituted benzene derivatives: Low temperature X-ray study on 1,3,5-trimethoxybenzene, and ab initio calculations on 1,3,5-triformylo - benzene and trimethoxy-benzene and the related di-substituted systems-Reference-Cited by-同舟云学术

The imbalanced kekule structure contributions in the ring in 1,3,5-trisubstituted benzene derivatives: Low temperature X-ray study on 1,3,5-trimethoxybenzene, and ab initio calculations on 1,3,5-triformylo - benzene and trimethoxy-benzene and the related di-substituted systems

Published:1996-08 Issue:34 Volume:52 Page:11379-11384
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Howard Sean T.,Krygowski Tadeusz Marek,Glówka Marek L.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference31 articles.

1. Is the delocalized .pi. system of benzene a stable electronic system?

2. Is delocalization a driving force in chemistry? Benzene, allyl radical, cyclobutadiene, and their isoelectronic species

3. The distortive tendencies of delocalized π electronic systems. Benzene, cyclobutadiene and related heteroannulenes

4. Influence of .sigma. and .pi. electrons on aromaticity

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